16814-17-8

Basic information

• Product Name: N-(p-methylbenzyl)hydroxylamine
• Synonyms: N-(p-methylbenzyl)hydroxylamine
• CAS NO: 16814-17-8
• Molecular Weight: 137.181
• Mol File: 16814-17-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-(p-methylbenzyl)hydroxylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(p-methylbenzyl)hydroxylamine(16814-17-8)
• EPA Substance Registry System: N-(p-methylbenzyl)hydroxylamine(16814-17-8)

Safety Data

• Hazardous Substances Data: 16814-17-8(Hazardous Substances Data)

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 146085-60-1 N-(p-methylbenzyl)-O-benzylhydroxylamine hydrochloride 
• 140451-62-3 O-benzyl oxime of 4-methylbenzaldehyde 
• 3235-02-7 p-methylbenzaldehyde oxime 
• 146085-66-7 N-(p-methylbenzyl)-O-benzyl-N-nitrosohydroxylamine 
• 104-81-4 4-Methylbenzyl bromide 
• 104-82-5 4-Methylbenzyl chloride 

Downstream Products

• 33863-77-3 N-(4-methylbenzyl)-4-methylaniline 
• 1391090-03-1 benzyl (2-(2,2,2-trifluoro-N-(4-methylbenzyl)acetamido)cyclopent-2-en-1-yl)carbamate 
• 1391090-17-7 N-cyclopentylidene-1-(p-tolyl)methanamine oxide 
• 1361055-79-9 (S)-2-(4-methylbenzyl)-3,5-diphenyl-2,3-dihydroisoxazole-4-carbaldehyde 
• 55606-34-3 α-Phenyl-N-p-methylbenzylnitron 
• 127213-34-7 4-methylbenzylazoxyoxysulfonyl(4-cyano)benzene 
• 127213-32-5 4-methylbenzylazoxyoxysulfonyl(4-methoxy)benzene 
• 396677-86-4 N-nitroso-N-(4-methylbenzyl)hydroxylamine 

Relevant articles and documents

Metal- and Base-Free Room-Temperature Amination of Organoboronic Acids with N-Alkyl Hydroxylamines

We have found that readily available N-alkyl hydroxylamines are effective reagents for the amination of organoboronic acids in the presence of trichloroacetonitrile. This amination reaction proceeds rapidly at room temperature and in the absence of added metal or base, it tolerates a remarkable range of functional groups, and it can be used in the late-stage assembly of two complex units.

Phase-transfer catalysis for the synthesis of hydroxylamines from oximes using benzyltriethylammonium borohydride in methanol and under solid-phase conditions

Effective phase-transfer catalysis methodologies for the reduction of oximes to hydroxylamines by a selective and versatile reducing agent, benzyltriethylammonium borohydride (BTEABH), in methanol and under solid-phase conditions are presented.

New NO donors with antithrombotic and vasodilating activities, Part 29. N-(1-cyanocyclohexyl)-C-phenylnitrones and glyoxaldinitrones.

Six N-(1-cyanocyclohexyl)-C-phenylnitrones 4a-f (4b-f for the first time) and 22 glyoxaldinitrones 7a-v were prepared and tested for antithrombotic (p.o. administration to rats, 60 mg/kg) effects. Both classes of compounds exhibit considerable antithrombo