75383-60-7

Basic information

• Product Name: (4-hydroxy-benzyl)carbamic acid benzyl ester
• Synonyms: (4-hydroxy-benzyl)carbamic acid benzyl ester
• CAS NO: 75383-60-7
• Molecular Weight: 257.289
• Mol File: 75383-60-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (4-hydroxy-benzyl)carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (4-hydroxy-benzyl)carbamic acid benzyl ester(75383-60-7)
• EPA Substance Registry System: (4-hydroxy-benzyl)carbamic acid benzyl ester(75383-60-7)

Safety Data

• Hazardous Substances Data: 75383-60-7(Hazardous Substances Data)

Upstream product

• 696-60-6 4-aminomethylphenol 
• 501-53-1 benzyl chloroformate 
• 83171-41-9 (4-(allyloxy)phenyl)methanamine 
• 767-00-0 4-cyanophenol 
• 33148-47-9 4-allyloxy-benzonitrile 
• 219501-50-5 N-benzyloxycarbonyl-4-allyloxy-benzylamine 

Downstream Products

• 914645-85-5 2-(S)-tert-butoxycarbonylamino-3-{4-[4-({[2-(1-isobutoxy-ethoxycarbamoyl)-benzo[b]thiophen-6-ylmethyl]-amino}-methyl)-phenoxy]-cyclohexyl}-propionic acid cyclopentyl ester 
• 914645-84-4 3-[4-(4-aminomethyl-phenoxy)-cyclohexyl]-2-(S)-tert-butoxycarbonylamino-propionic acid cyclopentyl ester 
• 914452-43-0 (S)-4-(4-aminomethyl-phenoxy)-2-tert-butoxycarbonylamino-butyric acid cyclopentyl ester 
• 914452-42-9 (S)-4-[4-(benzyloxycarbonylamino-methyl)-phenoxy]-2-tert-butoxycarbonylamino-butyric acid cyclopentyl ester 
• 914645-83-3 3-{4-[4-(benzyloxycarbonylamino-methyl)-phenoxy]-cyclohexyl}-2-(S)-tert-butoxycarbonylamino-propionic acid cyclopentyl ester 
• 75383-65-2 p-acetoxybenzylamine p-toluenesulfonate 
• 1054810-46-6 Acetic acid (2S,3R,4R,5S,6S)-4,5-diacetoxy-2-(4-aminomethyl-phenoxy)-6-methyl-tetrahydro-pyran-3-yl ester 
• 147821-50-9 N-ethoxythiocarbonyl-4-(2',3',4'-tri-O-acetyl-α-L-rhamnopyranosyloxy)-benzylamine 
• 147821-49-6 O-ethyl 4-[(α-L-rhamnosyloxy)benzyl]thiocarbamate 
• 147821-48-5 N-methoxythiocarbonyl-4-(2',3',4'-tri-O-acetyl-α-L-rhamnopyranosyloxy)-benzylamine 
• 219501-53-8 N-benzyloxycarbonyl-4-(2',3',4'-tri-O-acetyl-α-L-rhamnopyranosyloxy)-benzylamine 

Relevant articles and documents

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A compound selected from 14-O-[((Alkyl-, cycloalkyl-, heterocycloalkyl-, heteoroaryl-, or aryl)-sulfanyl)-acetyl]-12-epi-mutilins, or 14-O-[((Alkyl-, cycloalkyl-, heterocycloalkyl-, heteoroaryl-, or aryl)-oxy)-acetyl]-12-epi-mutilins, wherein 12-epi-mutilin is characterized in that the mutilin ring at position 12 is substituted by two substituents, the first substituent at position 12 of the mutilin ring is a methyl group which methyl group has the inverse stereochemistry compared with the stereochemistry of the methyl group at position 12 of the naturally occurring pleuromutilin ring, the second substituent at position 12 of the mutilin ring is a hydrocarbon group comprising at least one nitrogen atom and all other substituents of the mutilin ring having the same stereochemistry compared with the stereochemistry of the substituents at the corresponding positions in the naturally occurring pleuromutilin ring; optionally in the form of a salt and/or solvate, wherein the naturally occurring pleuromutilin is of formula processes for the preparation of such compounds and their use as pharmaceuticals.

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α-l-Rhamnosides of 4-hydroxy-benzyl compounds with nitrile, carbamate, and thiocarbamate groups occurring in Moringa oleifera leaf extracts and the α-l-rhamnoside of anisaldehyde derivatives were synthesised. Electrophilic activation of S-pent-4-enyl thiorhamnosides was applied for the construction of glycosidic linkages. Copyright (C) 1997 Elsevier Science Ltd.