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2-Pyridinamine, N-(5-chloro-2-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89660-11-7

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89660-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89660-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,6 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89660-11:
(7*8)+(6*9)+(5*6)+(4*6)+(3*0)+(2*1)+(1*1)=167
167 % 10 = 7
So 89660-11-7 is a valid CAS Registry Number.

89660-11-7SDS

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 N-(5-chloro-2-nitrophenyl)pyridin-2-amine

1.2 Other means of identification

Product number -
Other names -

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:89660-11-7 SDS

89660-11-7Relevant academic research and scientific papers

Cobalt-Catalyzed Regioselective Ortho C(sp2)-H Bond Nitration of Aromatics through Proton-Coupled Electron Transfer Assistance

Nageswar Rao, Desaboini,Rasheed, Sk.,Raina, Gaurav,Ahmed, Qazi Naveed,Jaladanki, Chaitanya Kumar,Bharatam, Prasad V.,Das, Parthasarathi

, p. 7234 - 7244 (2017/07/26)

A cobalt-catalyzed proton-coupled electron transfer (PCET) mediated regioselective ortho-specific nitration of aromatic C(sp2)-H bonds using chelation-assisted removable vicinal diamine directing groups was developed. The reaction proceeded under mild conditions in the presence of Co(OAc)2·4H2O as the catalyst with AgNO2 utilized as the nitro source as well as terminal oxidant in the presence of O2 as an external oxidant. No external base or additives were required for this process. Controlled experiments and mechanistic investigations with DFT calculations revealed that the reaction proceeds through a PCET promoted nitro functional group transfer pathway. Moreover, the produced compounds are valuable and pharmaceutically quite relevant.

RECEPTOR FUNCTION REGULATING AGENT

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Page/Page column 82-83, (2010/11/28)

The present invention relates to a GPR40 receptor function regulator comprising a fused imidazole compound represented by the formula: wherein each symbol is as defined in the specification, or a salt thereof or a prodrug thereof. The GPR40 receptor funct

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.

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