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62882-01-3

62882-01-3

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62882-01-3 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 58, p. 2631, 1993 DOI: 10.1021/jo00061a046

Check Digit Verification of cas no

The CAS Registry Mumber 62882-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,8 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62882-01:
(7*6)+(6*2)+(5*8)+(4*8)+(3*2)+(2*0)+(1*1)=133
133 % 10 = 3
So 62882-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H9N/c1-8-3-2-4-9-7-11-6-5-10(8)9/h2-7H,1H3

62882-01-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Methylisoquinoline

1.2 Other means of identification

Product number -
Other names 5-methylisoquinoline

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:62882-01-3 SDS

62882-01-3Relevant articles and documents

Acylation of o-Tolualdehyde Cyclohexylimines with N-Methoxy-N-methylamides (Weinreb's Amides). A New Synthesis of Isoquinolines

Flippin, Lee A.,Muchowski, Joseph M.

, p. 2631 - 2632 (1993)

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User-friendly methylation of aryl and vinyl halides and pseudohalides with DABAL-Me3

Cooper, Thea,Novak, Andrew,Humphreys, Luke D.,Walker, Matthew D.,Woodward, Simon

, p. 686 - 690 (2007/10/03)

An extremely technically simple cross-methylation of aryl and vinyl halides and pseudohalides using an air-stable adduct of trimethylaluminium with a Pd(0) catalyst supported by commercially available biarylphosphines gives excellent yields of methylated products (mainly > 95%). Reactions can be run with either 0.5 mol% catalyst or without requiring the exclusion of atmospheric oxygen or the drying of solvents in some cases. A wide variety of functional groups is tolerated including CN, OH, CO2R, CHO and NO2.

Antithrombotic amidinophenylalanine and amidinopyridylalanine derivatives

-

, (2008/06/13)

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