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27048-28-8

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27048-28-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27048-28-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,4 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27048-28:
(7*2)+(6*7)+(5*0)+(4*4)+(3*8)+(2*2)+(1*8)=108
108 % 10 = 8
So 27048-28-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H11ClN2/c13-10-4-6-11(7-5-10)15-9-12-3-1-2-8-14-12/h1-8,15H,9H2

27048-28-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-N-(pyridin-2-ylmethyl)aniline

1.2 Other means of identification

Product number -
Other names N-(4-chlorophenyl)pyridine-2-methylamine

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:27048-28-8 SDS

27048-28-8Relevant articles and documents

A half sandwich ruthenium(II) complex with n-4,6-dimethyl-2-pyrimidinylimidazole: Synthesis, crystal structure and application in N-Alkylation of amines with alcohols

Li, Hong-Mei,Xu, Chen,Wang, Zhi-Qiang,Fu, Wei-Jun

, p. 2557 - 2560 (2015/10/19)

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Fe2O3-supported nano-gold catalyzed one-pot synthesis of N-alkylated anilines from nitroarenes and alcohols

Peng, Qiling,Zhang, Yan,Shi, Feng,Deng, Youquan

supporting information; experimental part, p. 6476 - 6478 (2011/06/28)

Here, we show the one-step synthesis of N-alkylated anilines from nitrobenzenes and alcohols catalyzed by nano-gold catalyst. The yields to N-alkylated anilines were ~90% under mild conditions. The mechanism of this reaction was explored. It shows promise for clean and simple synthesis of N-alkylated anilines.

Identification and characterization of amino-piperidinequinolones and quinazolinones as MCHr1 antagonists

Blackburn, Christopher,LaMarche, Matthew J.,Brown, James,Che, Jennifer Lee,Cullis, Courtney A.,Lai, Sujen,Maguire, Martin,Marsilje, Thomas,Geddes, Bradley,Govek, Elizabeth,Kadambi, Vivek,Doherty, Colleen,Dayton, Brian,Brodjian, Sevan,Marsh, Kennan C.,Collins, Christine A.,Kym, Philip R.

, p. 2621 - 2627 (2007/10/03)

Several potent, functionally active MCHr1 antagonists derived from quinolin-2(1H)-ones and quinazoline-2(1H)-ones have been synthesized and evaluated. Pyridylmethyl substitution at the quinolone 1-position results in derivatives with low-nM binding potency and good selectivity with respect to hERG binding.

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