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869668-73-5

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869668-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869668-73-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,6,6 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 869668-73:
(8*8)+(7*6)+(6*9)+(5*6)+(4*6)+(3*8)+(2*7)+(1*3)=255
255 % 10 = 5
So 869668-73-5 is a valid CAS Registry Number.

869668-73-5SDS

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 1-(2-aminophenyl)-2-(2-bromophenyl)ethanone

1.2 Other means of identification

Product number -
Other names Ethanone,1-(2-aminophenyl)-2-(2-bromophenyl)

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:869668-73-5 SDS

869668-73-5Relevant articles and documents

Sequential palladium-catalysed C- and N-arylation reactions as a practical and general protocol for the synthesis of the first series of oxcarbazepine analogues

Carril, Mónica,SanMartin, Raul,Domínguez, Esther,Tellitu, Imanol

, p. 690 - 702 (2007/10/03)

The first series of oxcarbazepine analogues, starting from readily-available materials and through a high-yielding five-step sequence based on palladium catalysis, is reported. The so-obtained compounds incorporate not only a variety of substituents in both of?the aryl rings comprising the framework of an oxcarbazepine, but also involve the more challenging palladium-catalysed coupling of a number of heteroaromatic substrates. The addition of small amounts of water in some of the metal-catalysed processes showed a beneficial effect, highly increasing the selectivity of such reactions.

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