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25251-62-1

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25251-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25251-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,5 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25251-62:
(7*2)+(6*5)+(5*2)+(4*5)+(3*1)+(2*6)+(1*2)=91
91 % 10 = 1
So 25251-62-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H15BrN.BrH/c1-12(2,3)8-9-4-6-10(11)7-5-9;/h4-7H,8H2,1-3H3;1H/q+1;/p-1

25251-62-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-bromophenyl)methyl-trimethylazanium,bromide

1.2 Other means of identification

Product number -
Other names (4-Brom-benzyl)-trimethyl-ammonium,Bromid

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:25251-62-1 SDS

25251-62-1Relevant articles and documents

Real-time monitoring of a cobalt-mediated one-pot transition metal-catalyzed multicomponent reaction

Crotti, Ant?nio E. M.,Donate, Paulo M.,Previdi, Daniel,Scott McIndoe, J.

, (2020/04/15)

In this paper, pressurized sample infusion electrospray ionization mass spectrometry (PSI-ESI-MS) and FTIR spectroscopy were used to investigate the mechanism of a like-Barbier cobalt-mediated one-pot transition metal-catalyzed multicomponent reaction (MC

Benzylic Ammonium Ylide Mediated Epoxidations

Roiser, Lukas,Robiette, Rapha?l,Waser, Mario

supporting information, p. 1963 - 1968 (2016/08/10)

A high yielding synthesis of stilbene oxides using ammonium ylides has been developed. It turned out that the amine leaving group plays a crucial role as trimethylamine gives higher yields than DABCO or quinuclidine. The amine group also influences the diastereoselectivity, and detailed DFT calculations to understand the key parameters of these reactions have been carried out.

Micellar Dediazoniation: Dramatic Directive Effects on the Course of Reaction

Moss, Robert A.,Dix, Frank M.,Romsted, Laurence

, p. 5048 - 5050 (2007/10/02)

Rate constants and products are reported for the dediazoniation reactions of nonmicellar (p-diazoniobenzyl)trimethylammonium dibromide and micellar (p-diazoniobenzyl)dimethyl-n-hexadecylammonium dibromide in aqueous solutions at pH 4, 23 deg C, in the pre

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