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6,7-dihydro-3-methyl-5H-1-pyrindine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28712-61-0

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28712-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28712-61-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,7,1 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28712-61:
(7*2)+(6*8)+(5*7)+(4*1)+(3*2)+(2*6)+(1*1)=120
120 % 10 = 0
So 28712-61-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H11N/c1-7-5-8-3-2-4-9(8)10-6-7/h5-6H,2-4H2,1H3

28712-61-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-6,7-dihydro-5H-cyclopenta[b]pyridine

1.2 Other means of identification

Product number -
Other names 5-Methyl-2,3-cyclopentano-pyridin

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:28712-61-0 SDS

28712-61-0Downstream Products

28712-61-0Relevant academic research and scientific papers

Synthesis of alkyl- and aryl-substituted pyridines from (α,β-unsaturated) imines or oximes and carbonyl compounds

Vijn,Arts,Green,Castelijns

, p. 573 - 578 (2007/10/02)

Reaction of a variety of (α,β-unsaturated) imines or oximes with aliphatic aldehydes or cyclic ketones in the presence of a secondary amine afforded alkyl-, and/or aryl-, and/or cycloalkyl-substituted pyridines. To explain their formation, a hetero Diels-Alder reaction has been postulated, in which an 1-aza-1,3-butadiene reacts with an in situ generated enamine.

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