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87662-94-0

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87662-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87662-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,6 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87662-94:
(7*8)+(6*7)+(5*6)+(4*6)+(3*2)+(2*9)+(1*4)=180
180 % 10 = 0
So 87662-94-0 is a valid CAS Registry Number.

87662-94-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name O-benzoyl-N,N-dibutylhydroxylamine

1.2 Other means of identification

Product number -
Other names N-(benzoyloxy)dibutylamine

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:87662-94-0 SDS

87662-94-0Relevant articles and documents

Copper- and Cobalt-Catalyzed Syntheses of Thiophene-Based Tertiary Amines

Bouarfa, Salima,Gra?l, Simon,Ivanova, Maria,Langlais, Timothy,Bentabed-Ababsa, Ghenia,Lassagne, Frédéric,Erb, William,Roisnel, Thierry,Dorcet, Vincent,Knochel, Paul,Mongin, Florence

, p. 3244 - 3258 (2019/06/08)

Thienylzinc halides and related compounds prepared by deprotonation followed by transmetalation were used in copper-catalyzed amination using N-benzoyloxy secondary amines. By extending the reaction to 1,5-naphthyridine, it was showed that the competitive dimer formation observed in the case of thiophenes was linked with the low stability of some thienylamines rather than homocoupling. Interestingly, thienylzinc halides and related compounds prepared by transmetalation of thienylmagnesium halides, either prepared from their bromo-precursors or generated by deprotometalation, were satisfactorily employed in cobalt-catalyzed aminations. Finally, aminothiophenes were involved in copper-catalyzed mono- and di-N-arylations, affording differently substituted di- and triphenylamines.

Improved Oxidation of Amines with Dibenzoyl Peroxide

Biloski, Alan J.,Ganem, Bruce

, p. 537 - 538 (2007/10/02)

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