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5H-Cyclopenta[b]pyridine-2-carboxylic acid, 6,7-dihydro-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

221137-08-2

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221137-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221137-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,1,3 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 221137-08:
(8*2)+(7*2)+(6*1)+(5*1)+(4*3)+(3*7)+(2*0)+(1*8)=82
82 % 10 = 2
So 221137-08-2 is a valid CAS Registry Number.

221137-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 6,7-dihydro-5H-cyclopenta[b]pyridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names 6,7-Dihydro-5H-[1]pyrindine-2-carboxylic acid methyl ester

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:221137-08-2 SDS

221137-08-2Downstream Products

221137-08-2Relevant academic research and scientific papers

Cycloadditions of noncomplementary substituted 1,2,3-triazines

Anderson, Erin D.,Duerfeldt, Adam S.,Zhu, Kaicheng,Glinkerman, Christopher M.,Boger, Dale L.

, p. 5084 - 5087 (2014)

The scope of the [4 + 2] cycloaddition reactions of substituted 1,2,3-triazines, bearing noncomplementary substitution with electron-withdrawing groups at C4 and/or C6, is described. The studies define key electronic and steric effects of substituents impacting the reactivity, mode (C4/N1 vs C5/N2), and regioselectivity of the cycloaddition reactions of 1,2,3-triazines with amidines, enamines, and ynamines, providing access to highly functionalized heterocycles.

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