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809231-07-0

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809231-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 809231-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,9,2,3 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 809231-07:
(8*8)+(7*0)+(6*9)+(5*2)+(4*3)+(3*1)+(2*0)+(1*7)=150
150 % 10 = 0
So 809231-07-0 is a valid CAS Registry Number.

809231-07-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-2-ethenyl-4-methylaniline

1.2 Other means of identification

Product number -
Other names Benzenemethanamine,N-(2-ethenyl-4-methylphenyl)

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:809231-07-0 SDS

809231-07-0Downstream Products

809231-07-0Relevant articles and documents

Indole synthesis by controlled carbolithiation of o-aminostyrenes

Kessler, Albane,Coleman, Claire M.,Charoenying, Patchanee,O'Shea, Donal F.

, p. 7836 - 7846 (2007/10/03)

An effective synthesis of the functionalized indole ring system has been developed from substituted o-aminostyrene starting material. Our methodology involves a novel cascade reaction sequence of alkyllithium addition to the styrene double bond and subsequent trapping of the intermediate organolithium with a suitable electrophile, followed by an in situ ring closure and dehydration to generate the indole ring. This new reaction sequence allows for the introduction of molecular diversity at all positions on the indole scaffold. The procedure was shown to be successful with a range of both C and N substituents on the o-aminostyrenes. The reaction sequence was tolerant to the reactivity range of alkyllithiums such as tert-, sec-, and n-butyllithium. The electrophiles used were DMF, which generated indole products with C-2 unsubstituted, and nitriles, which incorporated the nitrile substituent at C-2. The o-aminostyrene starting materials were generated by a Pd-catalyzed cross-coupling reaction of a vinyl boronic acid equivalent with the readily available substituted o-bromoanilines.

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