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Pyridine, 1,2-dihydro-1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33707-38-9

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33707-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33707-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,0 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33707-38:
(7*3)+(6*3)+(5*7)+(4*0)+(3*7)+(2*3)+(1*8)=109
109 % 10 = 9
So 33707-38-9 is a valid CAS Registry Number.

33707-38-9SDS

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 1-methyl-2H-pyridine

1.2 Other means of identification

Product number -
Other names N-Methyl-1,2-dihydropyridin

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:33707-38-9 SDS

33707-38-9Upstream product

33707-38-9Relevant academic research and scientific papers

Synthesis and pharmacological properties of 2-azabicyclooctane derivatives representing conformational restricted isopethidine analogues

Cardellini, Mario,Cingolani, Gian Mario,Claudi, Francesco,Gulini, Ugo,Cantalamessa, Franco,Venturi, Fabrizio

, p. 1 - 4 (1987)

The synthesis and preliminary pharmacological evaluation of the epimeric 2-methyl-6-phenyl-6-carbethoxy-2-azabicyclooctanes, representing conformationally restricted isopethidine analogues, are reported. 2-azabicyclooctanes / isopethidine analogues / structure-activity relationship

SELECTIVE REDUCTION OF IMONIUM SALTS BY SODIUM HYDROGEN TELLURIDE

Barton, Derek H. R.,Fekih, Abdelwaheb,Lusinchi, Xavier

, p. 3693 - 3696 (2007/10/02)

Sodium hydrogen telluride reduces imonium salts efficiently at room temperature in ethanol.The products of the reaction depend upon the pH.Under alkaline pH only dihydro-derivatives are formed.Under acid pH (6-7) the products depend on the structure of the salt.The tellurium can be recovered quantitatively.

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