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42459-12-1

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42459-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42459-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,4,5 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42459-12:
(7*4)+(6*2)+(5*4)+(4*5)+(3*9)+(2*1)+(1*2)=111
111 % 10 = 1
So 42459-12-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H13N3/c1-14-10(7-12)4-5-11(14)9-3-2-6-13-8-9/h2-3,6,8,10-11H,4-5H2,1H3

42459-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-5-pyridin-3-ylpyrrolidine-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 5'-cyanonicotine

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:42459-12-1 SDS

42459-12-1Relevant articles and documents

Letter: Nicotine chemistry. 5'-cyanonicotine.

Sanders,DeBardeleben,Osdene

, p. 2848 - 2849 (1975)

-

TiO2Nanoparticles Functionalized with Non-innocent Ligands Allow Oxidative Photocyanation of Amines with Visible/Near-Infrared Photons

Nauth,Schechtel, Eugen,D?ren, René,Tremel, Wolfgang,Opatz, Till

supporting information, p. 14169 - 14177 (2018/10/26)

Photosynthesis is an efficient mechanism for converting solar light energy into chemical energy. We report on a strategy for the aerobic photocyanation of tertiary amines with visible and near-infrared (NIR) light. Panchromatic sensitization was achieved

NICOTINE COMPOUNDS AND ANALOGS THEREOF, SYNTHETIC METHODS OF MAKING COMPOUNDS, AND METHODS OF USE

-

Page/Page column 43, (2012/03/26)

Embodiments of the present disclosure provide for compounds such as those shown in FIG. 1.1 (compounds A, B, C, and D), 2'substituted nicotine compounds, azetidine compounds, ether linked nicotine compounds (FIG. 1.2, compounds E, F, G, and H), methods of synthesis of the compounds, methods of treatment of a condition using compounds A, B, C, D, 2'substituted nicotine compounds, azetidine compounds, or ether linked nicotine compounds, methods of selectively stimulating alpha7 nAChR and/or alpha4beta2 receptors, and the like.

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