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147293-17-2

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147293-17-2 Usage

Chemical Properties

Yellow Solid

Uses

N-Methyl-5-nitro-6-isoquinolinamine (cas# 147293-17-2) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 147293-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,9 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 147293-17:
(8*1)+(7*4)+(6*7)+(5*2)+(4*9)+(3*3)+(2*1)+(1*7)=142
142 % 10 = 2
So 147293-17-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H9N3O2/c1-11-9-3-2-7-6-12-5-4-8(7)10(9)13(14)15/h2-6,11H,1H3

147293-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-5-nitroisoquinolin-6-amine

1.2 Other means of identification

Product number -
Other names 6-Isoquinolinamine,N-methyl-5-nitro

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:147293-17-2 SDS

147293-17-2Relevant articles and documents

Amination of Some Nitroisoquinolines with Liquid Methylamine/Potassium Permanganate

Wozniak, Marian,Nowak, Krystyna

, p. 355 - 360 (2007/10/02)

5-Nitro-, 3-methyl-5-nitro-, 5,7-dinitro-, 5-chloro-8-nitro- and 8-chloro-5-nitroisoquinoline (1a-e) as well as 5-nitroisoquinoline N-oxide (1f) are aminated with a liquid methylamine solution of potassium permanganate (LMA/PP) to the corresponding mono- or mono- and bis(methylamino)-substituted nitro compounds 2 (a-m). 1-Nitroisoquinoline (1g) is aminated with LMA/PP to 1-(methylamino)isoquinoline (2n).Quantum-chemical calculations for some mononitroisoquinolines suggest that, in general, the experimentally observed regioselectivity of the amination is controlled by an interaction of frontal molecular orbitals (FMO) of the reagents. - Key Words: Methylaminations / Calculations, FMO / Isoquinolines / Aminations / Nitro compounds

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