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JPS539743A |
PURPOSE: N-Benzoly-N'-4-fluorophenylthiourea I.
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JPS539742A |
PURPOSE: Phenylthiourea derivatives I (X is phenyl and or phenyl substituted by at least one group selected from halogen, lower alkyl, etc.), e.g. N-monofluoroacetyl-N'-trichlorophenylthiourea.
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JPS539744A |
Compounds of the formula wherein each X is independently selected from a group consisting of hydrogen, chlorine, bromine, alkyl, and haloalkyl, said alkyl containing 1 to 6 carbon atoms and said haloalkyl of 1 to 6 carbon atoms containin...
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JPS539751A |
There are provided certain substituted-1,2,3,4-tetrahydro-4-imino-1-naphthylureas, methods of preparation thereof, and methods of use of said naphthylureas for enhancing feed efficiency and for promoting the growth rate of veterinary hom...
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JPS537645A |
The compound of formula in which R, R1, and X have the meanings shown in Claim 1, is obtained by treatment of a compound of formula with a base, and then by carrying out a treatment with a compound having the formula RX<2> in which X<2> ...
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JPS534540A |
PURPOSE: To provide a photographic material for diffusion copying, which is capable of forming image without distortion, excellent storage stability and improved in photostability with increased color concentration as well as color purit...
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JPS532420A |
S-(Aminoalkyl)isothioureas which have immunosuppressant activity. Two specific compounds are 2-(3-dimethylaminopropylthio)-2-imidazoline and N,N'-dimethyl-S-(3-dimethylaminopropyl)isothiourea.
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JPS52128348A |
PURPOSE: α-Chlorocarboxylic acid derivatives I[R is lower alkyl, (substituted) phebyl;Y is II (R1-2 are lower alkylene or a bond;L1-2 are H or lower alkyl); R3 is H or lower alkyl; X is O or S;Z is lower alkyl or (substituted) amino], e...
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JPS52128332A |
Antihypertensively active thiourea derivatives of the formulas I and II wherein R, R1, R2, R3 and X are as hereinafter described, AS WELL AS A METHOD OF USING A COMPOUND OF THE FORMULA III wherein R1', R2', R3 and X are as previously des...
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JPS52118426A |
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JPS5293742A |
4-(Sulfamoyl-phenyl)-4-hydroxy-2-imino-thiazolidine-derivati
ves having salidiuretic activity and a process for their manufacture.
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JPS5289645A |
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JPS5285141A |
Certain substituted alpha -halo and alpha -mercaptophenylacetic acids and substituted phenylacetic acids having in alpha -position a sulfur-containing group, a cyano group, or an amino group, their substantially non-toxic esters, salts, ...
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JPS5277015A |
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JPS5268128A |
The compounds are substituted S-(aminoalkyl)isothioureas which are histamine H2-antagonists. Two specific compounds of the present invention are S-[6-(N'-methylthioureido)hexyl]isothiourea and S-[5-(N'-cyano-N''-methylguanidino)pentyl]is...
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JPS5268144A |
Novel S-alkylthio or S-arylthio N-phenyl isothiourea derivs. are cpds. of formula (I) (where R1 and R2 are H, halogen, 1-4C alkyl or NO2; R3 is 1-4C alkyl; R4 is H or 1-4C alkyl; and R5 is opt. halo-substd. 1-10C alkyl, or is phenyl or n...
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JPS5268145A |
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JPS5218255B1 |
Compounds of the formula wherein A is a hydrogen atom, a halogen atom, a methyl group, or a methoxy group; B is a hydrogen atom, a halogen atom, a methyl group, or a methoxy group, with the proviso that A and B ar not both a hydrogen ato...
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JPS5217095B2 |
N-(4-halobenzyl)-N-sec. alkyl-N'-phenylthioureas of the formula in which R is a C1-C6 alkyl radical, and X is a halogen atom.
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JPS5213741B2 |
A method for developing a diazo-type photographic light-sensitive material containing at least one light-sensitive diazonium compound (Component A) selected from the compounds represented by the general formula; WHEREIN R1 and R2 each re...
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JPS5217445A |
Di-[2-thioureido-(N-Alkoxycarbonyl)-N-phenylureides] of the formula +TR wherein R1 is hydrogen, halogen, or an alkoxy or alkyl radical having 1 to 4 C atoms, R2 is an alkyl radical having 1 to 4 C atoms, and R3 is an alkylene radical hav...
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JPS5212131A |
Miticidally active compounds, which are defined by the following generic formula wherein R and R1 in general are selected from the group consisting of benzhydryl, 3'-(2'-ethylhexoxy)-propyl, allyl, cyclohexyl, cycloheptyl, and alkyl, are...
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JPS527980A |
1435585 6-Amino-s-triazin-2,4[1H,3H]-dione derivatives E I DU PONT DE NEMOURS & CO 23 May 1973 [24 May 1972 5 April 1973 (2)] 24677/73 Headings A5E E1C5J E1C5P E1C5M E1C14A E1C15D3 E1A3B ElA3Cand E1A5B3 Novel compounds have the Formula I...
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JPS525713A |
PURPOSE: Penicillamine derivatives I (where R1 is H or lower alkyl; R2 is alkyl, alkenyl, cycloalkyl, etc.), e.g. DL-N, S-bis-(methyl-carbamoyl)penicillamine ethylester.
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JPS51149240A |
PURPOSE: 3-Substituted aminophenylacetic acid derivatives or their lower alkyl esters or their salts of formula I[where R1 is lower alkyl, lower alkenyl or lower alkynyl; R2 is H or lower alkyl; R3 is represented by the formula -COR4, fo...
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JPS51146448A |
Tetrahydronaphthylureas of formula (I), their racemic mixture, cis and trans isomers and when U = CHOR6 their optical isomers, are novel cpds. (where X = O or S; U = R1,R2 independently = H or 1-4C alkyl; R3 = H, 1-4C alkyl, 3-5C alkynyl...
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JPS51143690A |
A process for the production of new benzo-2,4-thiazepines of formula I, **(See formula)** where each of R1 and R2, independently, means hydrogen, halogen, trifluoromethyl, a lower alkoxy group or a lower alkyl group, R3 is hydrogen, a lo...
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JPS51125763A |
Dermal protective compositions are disclosed which comprise a pharmaceutical extending medium having incorporated therein a substantive, dermally non-irritating compound which is a polyfunctional organic molecule containing one or more f...
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JPS5136736B2 |
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JPS51113843A |
Iso-(thio)-urea derivatives of the formula wherein R1 and R2 each represent C1-C5-alkyl or phenyl or benzyl mono-, di- or trisubstituted by halogen, trifluoromethyl, nitro and/or methyl, and X represents oxygen or sulphur, processes for ...
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JPS51114206A |
A method for increasing the yield of rice crops involving application of an s-triazinedione such as 3-(4-chlorophenyl)-6-methoxy-s-triazine-2,4(1H,3H)-dione to the seed, seedlings, or soil in which the seed or seedlings are planted.
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JPS5134451B2 |
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JPS5134450B2 |
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JPS51105034A |
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JPS5133173B2 |
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JPS51101920A |
Antimicrobial compounds are disclosed having the formula:
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JPS5124506B2 |
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JPS5170748A |
Benzene derivatives of the formula: I wherein R1 represents alkyl, R2 represents a group -SR3, -SOR3, -SO2R3, -OR3, -SCONH2, -SCN or -T(CH2)mT1R4 [wherein R3 represeents alkyl, cycloalkyl, alkenyl, alkynyl, aralkyl, unsubstituted or subs...
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JPS5115097B2 |
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JPS5148428A |
1448165 1 - Substituted - 5 - (substituted phenyl) - 3 - methyl - 1,3,5 - triazapenta - 1,4- dienes and their acaricidal compositions PFIZER Ltd 21 Aug 1975 [23 Aug 1974] 37232/74 Heading C2C The invention comprises compounds of general ...
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JPS5112689B2 |
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JPS5136434A |
N-[2-(Substituted amido)phenyl]-N'-carbonyl-S-substituted isothioureas bearing an optionally substituted phenoxy, phenylthio, phenylsulfinyl or phenylsulfonyl group in the 4- or 5-position of the 2-(substituted amido)-phenyl group are an...
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JPS515374B2 |
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JPS511643A |
New 3-amino-phenylacetic acid compounds of the formula: (I) wherein X is hydrocarbyloxy or hydrocarbylthio optionally substituted by halogen, alkoxy, aryloxy, alkylmercapto or arylmercapto, or X is mono- or disubstituted amino, or repres...
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JPS50160235A |
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JPS5034610B2 |
This invention relates to a method for combatting rodents (especially animals which belong to Muridae) comprising applying a rodenticidally effective amount of a compound of general formula (1) WHEREIN R1 is hydrogen or an alkyl group, R...
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JPS50129501A |
Secondary-aliphatic alpha -substituted azoalkanes of the formula where n is 1 or 2, R' and R'' are hydrocarbo, R1 and R2 are hydrocarbo or heterocyclic or joined to form a cyclic hydrocarbon group and X is selected from Cl, Br, CN, OH, N...
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JPS50126829A |
1463251 Isothiourea derivatives STAUFFER CHEMICAL CO 19 Feb 1975 [29 March 1974] 6974/75 Headings C2C and C2P [Also in Division A5] Isothiourea derivatives, some of which are novel, of the formula (R-N=C(SR 1 )NHR 2 ) n X, wherein n is 1...
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JPS5030612B2 |
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JPS50116616A |
Benzene ring substituted benzimidazole-2-carbamate derivatives represented by the formula:
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