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phenylalanyl adenylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35874-27-2

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35874-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35874-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,7 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35874-27:
(7*3)+(6*5)+(5*8)+(4*7)+(3*4)+(2*2)+(1*7)=142
142 % 10 = 2
So 35874-27-2 is a valid CAS Registry Number.

35874-27-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Phe-O-AMP

1.2 Other means of identification

Product number -
Other names [5']Adenylsaeure-L-phenylalanin-anhydrid

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:35874-27-2 SDS

35874-27-2Downstream Products

35874-27-2Relevant articles and documents

Amino acid dependent formation of phosphate anhydrides in water mediated by carbonyl sulfide

Leman, Luke J.,Orgel, Leslie E.,Ghadiri, M. Reza

, p. 20 - 21 (2006)

Carbonyl sulfide (COS), a component of volcanic gas emissions and interstellar gas clouds, is shown to be an efficient condensing agent in the context of phosphate chemistry in aqueous solutions. We report that high-energy aminoacyl-phosphate anhydrides a

31P NMR study on aminoacylatiqn of 5′-AMP and its analogs

Moriguchi, Tomohisa,Yanagi, Terukazu,Wada, Takeshi,Sekine, Mitsuo

, p. 1859 - 1865 (2007/10/03)

The progress of aminoacylation of 5′-AMP with amino acids in the presence of several condensing reagents was monitored by 31P NMR. The resulting products were identified on the basis of their 31P NMR chemical shifts. The aminoacylati

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