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Methanesulfonic acid, trifluoro-, 5-[[(4-methylphenyl)sulfonyl]amino]-6-(phenylmethyl)pyrazinyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

671240-61-2

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671240-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 671240-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,1,2,4 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 671240-61:
(8*6)+(7*7)+(6*1)+(5*2)+(4*4)+(3*0)+(2*6)+(1*1)=142
142 % 10 = 2
So 671240-61-2 is a valid CAS Registry Number.

671240-61-2SDS

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 5-N-(p-toluenesulfonyl)amide-6-benzyl-2-O-trifluoromethanesulfonyloxy-pyrazine

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:671240-61-2 SDS

671240-61-2Relevant academic research and scientific papers

Suzuki-Miyaura coupling for general synthesis of dehydrocoelenterazine applicable for 6-position analogs directing toward bioluminescence studies

Phakhodee, Wong,Toyoda, Mitsuko,Chou, Chun-Ming,Khunnawutmanotham, Nisachon,Isobe, Minoru

scheme or table, p. 1150 - 1157 (2011/03/21)

Synthesis of coelenterazine analogs is in recent demand to supply more luminescent compounds with reasonable stability as substrate for the photoprotein manipulated in a living cells or particular organelle. There are limited methods for the synthesis of

Novel synthetic route of aryl-aminopyrazine

Kuse, Masaki,Kondo, Nobuhiro,Ohyabu, Yuki,Isobe, Minoru

, p. 835 - 840 (2007/10/03)

We report a novel synthetic route of aryl-aminopyrazine through a new cyclization reaction by using a hydroxylamine. Starting from Boc-glycine and aminonitrile, the aminopyrazine ring was prepared in several steps. After trifluoromethane sulfonylation of the aminopyrazinone, the resultant triflate was subjected to Suzuki-Miyaura coupling reaction with aryl boronic acid to afford coelenteramine.

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