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61206-56-2

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61206-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61206-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,0 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61206-56:
(7*6)+(6*1)+(5*2)+(4*0)+(3*6)+(2*5)+(1*6)=92
92 % 10 = 2
So 61206-56-2 is a valid CAS Registry Number.

61206-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name isoquinolin-2-ium-2-yl(phenyl)methanone,chloride

1.2 Other means of identification

Product number -
Other names Isoquinolinium,2-benzoyl-,chloride

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:61206-56-2 SDS

61206-56-2Relevant articles and documents

Zn-alkynylide additions to acyl iminiums

Fischer, Christian,Carreira, Erick M.

, p. 1497 - 1499 (2004)

A new addition reaction of zinc-alkynylides to M-acyl and N-phosphinoyl iminiums is reported. These can be prepared in situ from imines with acid halides in the presence of a Zn-acetylide. The reaction is general with regard to imine, alkyne, and acid hal

Reissert Compound Studies. LXIV. Reissert Compound and Other Products From an Isolated N-Benzoylisoquinolinium Triflate Salt

Duarte, F. F.,Popp, F. D.

, p. 1801 - 1804 (2007/10/02)

In the presence of trimethylsilyl trifluoromethanesulfonate, a methylene chloride solution of isoquinoline and benzoyl chloride gave N-benzoylisoquinolinium triflate (3) and N-H-isoquinolinium triflate (4).Depending on the reaction conditions, reaction of 3 may occur on the isoquinoline ring yielding a Reissert compound and 1,2-dihydroisoquinoline species.Otherwise, reactions transpire on the carbonyl of 3 to give an amide, an ester, and an anhydride.

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