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65745-70-2

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65745-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65745-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,4 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65745-70:
(7*6)+(6*5)+(5*7)+(4*4)+(3*5)+(2*7)+(1*0)=152
152 % 10 = 2
So 65745-70-2 is a valid CAS Registry Number.

65745-70-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-6-nitroquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,5-methyl-6-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:65745-70-2 SDS

65745-70-2Downstream Products

65745-70-2Relevant articles and documents

Selective ortho methylation of nitroheteroaryls by vicarious nucleophilic substitution

Achmatowicz, Michal,Thiel, Oliver R.,Gorins, Gilles,Goldstein, Corinne,Affouard, Caroline,Jensen, Randy,Larsen, Robert D.

, p. 6793 - 6799 (2008/12/22)

(Chemical Equation Presented) An efficient and scalable three-step one-pot approach to 6-methyl-5-nitroisoquinoline (1) from inexpensive 5-nitroisoquinoline, utilizing the vicarious nucleophilic substitution (VNS) as a key step, is described. The optimized reaction conditions can be applied to a limited number of other aromatic and heteroaromatic nitro compounds. Attempts to understand the observed selectivity in the VNS step led to the discovery of two new reaction pathways under VNS conditions, one leading to an isoxazole and the other resulting in the formal cyclopropanation of an aromatic nitro compound.

Reactivity of Nitroarenes towards Grignard Reagents; General Synthesis of Alkyl-Chloro Compounds in Aromatic Bicyclic Systems

Bartoli, Giuseppe,Bosco, Marcella

, p. 616 - 617 (2007/10/02)

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