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127073-69-2

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127073-69-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127073-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,7 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 127073-69:
(8*1)+(7*2)+(6*7)+(5*0)+(4*7)+(3*3)+(2*6)+(1*9)=122
122 % 10 = 2
So 127073-69-2 is a valid CAS Registry Number.

127073-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(allyl)(benzyl)amino]acetonitrile

1.2 Other means of identification

Product number -
Other names Acetonitrile, 2-?[(phenylmethyl)?-?2-?propen-?1-?ylamino]?-

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:127073-69-2 SDS

127073-69-2Relevant articles and documents

Palladium-catalyzed chemoselective intramolecular cyclization of bromoanilinoalkenenitriles

Yang, Chau-Chen,Tai, Huo-Mu,Sun, Pei-Jiun

, p. 2843 - 2850 (2007/10/03)

α-(o-Bromoanilino)alkenenitriIes 1a-f and 2a-e and α-(N-alkenylamino)-β-(o-bromophenyl)-propanenitriles 7a-c and 8a-c undergo palladium-catalyzed conversion into o-(methylamino)benzonitrile 12, o-[(alkenylamino)ethenyl]benzonitriles 24a-c, N-alkenylanilines 26b, 26c, 3-benzazepines 29a, 29c, 31a and 32a, γ-carbolines 36 and pyrrolo[3,2-b]indole 45. The reactions involve intramolecular additions of arylpalladium to the cyano group and subsequent processes such as cyano group transposition, hydrolysis, electrocyclization, ethyl group transfer and oxidative aromatization. A general mechanism for the palladium-catalyzed arylation of a cyano group is proposed.

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