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ethyl 1-Methylindole-6-carboxylate
Cas No: 202745-74-2
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ZHEJIANG JIUZHOU CHEM CO.,LTD
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Ethyl 1-methyl-1H-indole-6-carboxylate
Cas No: 202745-74-2
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ENAO Chemical Co, Limited
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ethyl 1-Methylindole-6-carboxylate
Cas No: 202745-74-2
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Chemical Technology Co.,LTD
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ETHYL 1-METHYL-1H-INDOLE-6-CARBOXYLATE
Cas No: 202745-74-2
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coolpharm Ltd
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202745-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 202745-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,7,4 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 202745-74:
(8*2)+(7*0)+(6*2)+(5*7)+(4*4)+(3*5)+(2*7)+(1*4)=112
112 % 10 = 2
So 202745-74-2 is a valid CAS Registry Number.

202745-74-2SDS

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	Ethyl 1-methyl-1H-indole-6-carboxylate

1.2 Other means of identification

Product number	-
Other names	5-carbaldehyde-N-methylindole

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:202745-74-2 SDS

202745-74-2Upstream product

202745-74-2Downstream Products

202745-74-2Relevant articles and documents

Electrochemically Enabled C3-Formylation and -Acylation of Indoles with Aldehydes

Yang, Liquan,Liu, Zhaoran,Li, Yujun,Lei, Ning,Shen, Yanling,Zheng, Ke

supporting information, p. 7702 - 7707 (2019/10/19)

Reported herein is an effective strategy for oxidative cross-coupling of indoles with various aldehydes. The strategy is based on a two-step transformation via a well-known Mannich-type reaction and a C-N bond cleavage for carbonyl introduction. The key step - the C-N bond cleavage of the Mannich product - was enabled by electrochemistry. This strategy (with over 40 examples) ensures excellent functional-group tolerance as well as late-stage functionalization of pharmaceutical molecules.

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CAS

202745-74-2