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41010-66-6

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41010-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41010-66-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,1 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41010-66:
(7*4)+(6*1)+(5*0)+(4*1)+(3*0)+(2*6)+(1*6)=56
56 % 10 = 6
So 41010-66-6 is a valid CAS Registry Number.

41010-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-chlorophenyl)-3-nitropyridin-2-amine

1.2 Other means of identification

Product number -
Other names (2-chloro-phenyl)-(3-nitro-pyridin-2-yl)-amine

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:41010-66-6 SDS

41010-66-6Relevant articles and documents

Imidazopyridine derivatives as PI3K inhibitors

-

Page/Page column 44, (2012/11/13)

New imidazopyridine derivatives having the chemical structure of formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Phosphoinositide 3-Kinases (PI3Ks)

The Preparation of All the Monochloro-α-carbolines and the Assignment of the 13C N.M.R. Spectrum of α-Carboline

Mohamed, Murtedsa bin,Parrick, John

, p. 577 - 593 (2007/10/02)

The five previously unknown chloro-α-carbolines are prepared, the 1H n.m.r. spectra of the chloro-α-carbolines are described, and the 13C n.m.r. spectrum of α-carboline is assigned.

3-Phenyl,3H 1,2,3 triazolo[4,5-b]pyridines

-

, (2008/06/13)

3H-1,2,3-Triazolo[4,5-b]pyridines substituted in the 3-position have utility as analgesic, anti-inflammatory and anti-pyretic agents. They are prepared by diazotization of a 3-amino-2-(substitute) aminopyridine.

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