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Benzenamine, N-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75841-12-2

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75841-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75841-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,4 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75841-12:
(7*7)+(6*5)+(5*8)+(4*4)+(3*1)+(2*1)+(1*2)=142
142 % 10 = 2
So 75841-12-2 is a valid CAS Registry Number.

75841-12-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name O-benzyl N-phenyl hydroxylamine

1.2 Other means of identification

Product number -
Other names O-benzyl-N-phenylhydroxylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:75841-12-2 SDS

75841-12-2Relevant academic research and scientific papers

Skeletal diversity via Pd(0) catalysed three-component cascades of allene and halides or triflates with protected hydroxylamines and formamide

Elboray, Elghareeb E.,Gao, Chuanjun,Grigg, Ronald

body text, p. 3103 - 3111 (2012/06/01)

The reactions of allene gas (1 atm) and of 1,1-dimethylallene with a range protected hydroxylamines and formamide with aryl/heteroaryl iodides, bromides and triflates under Pd(0) catalysis lead to a skeletally diverse range of products in good yield. The

Equilibrium acidities and homolytic bond dissociation energies of N-H and/or O-H bonds in N-phenylhydroxylamine and its derivatives

Bordwell, Frederick G.,Liu, Wei-Zhong

, p. 8777 - 8781 (2007/10/03)

The equilibrium acidities (pK(HA) values) in DMSO of the following hydroxylamines have been measured: (1) N-phenylhydroxylamine and its p-bromo and p-cyano derivatives, (2) N-benzyl-N-phenylhydroxylamine and its p-bromo and p-cyano derivatives, (3) O-benzyl-N-phenylhydroxylamine, (4) N-benzoylphenylhydroxylamine and its p-bromo and p-cyano derivatives, and (5) N-hydroxylpiperidine. The BDEs of the O-H and/or N-H bonds in these 11 weak acids have been estimated by combining their pK(HA) values with the oxidation potentials of their conjugate bases according to the following equation: BDE(HA) = 1.37pK(HA) + 23.1E(ox)(A-) + 73.3 kcal/mol.

Formation d'hydroxy-5 methyl-5 isoxazolidinones-3 par action du dicetene sur les hydroxylamines

Perronnet, Jacques,Girault, Pierre,Demoute, Jean-Pierre

, p. 727 - 731 (2007/10/02)

The reaction of diketene with N-monosubstituted hydroxylamines provides cyclic derivatives of the 5-hydroxy-5-methylisoxazolidin-3-one type.

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