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302912-35-2

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302912-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 302912-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,9,1 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 302912-35:
(8*3)+(7*0)+(6*2)+(5*9)+(4*1)+(3*2)+(2*3)+(1*5)=102
102 % 10 = 2
So 302912-35-2 is a valid CAS Registry Number.

302912-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chloro-1,2,3,4-tetrahydrocyclopenta[b]indole

1.2 Other means of identification

Product number -
Other names 7-Chloro-1,2,3,4-tetrahydrocyclopent[b]indole

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:302912-35-2 SDS

302912-35-2Downstream Products

302912-35-2Relevant articles and documents

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Massey,Plant

, p. 1990,1994 (1931)

-

Efficient synthesis of indoles using [3,3]-sigmatropic rearrangement of N-trifluoroacetyl enehydrazines

Miyata, Okiko,Takeda, Norihiko,Kimura, Yasuo,Takemoto, Yoshiji,Tohnai, Norimitsu,Miyata, Mikiji,Naito, Takeaki

, p. 3629 - 3647 (2007/10/03)

[3,3]-Sigmatropic rearrangement of N-trifluoroacetyl enehydrazines provides a novel method for the construction of indoles. N-Trifluoroacetyl enehydrazine having a cyclopentene ring smoothly underwent [3,3]-sigmatropic rearrangement followed by cyclizatio

Fischer indole synthesis in the absence of a solvent

Matsumoto, Kiyoshi,Tanaka, Akinori,Yukio, Ikemi,Hayashi, Naoto,Toda, Mitsuo,Bulman, Robert A.

, p. 9 - 12 (2007/10/03)

The traditional Fischer synthesis of indoles has been investigated and it has been shown that the reaction proceeds in good yield in the absence of a solvent.

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