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1H-Pyrrole-1-propanoic acid, 2,5-dihydro-2,5-dioxo-, pentafluorophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138194-55-5

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138194-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138194-55-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,9 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138194-55:
(8*1)+(7*3)+(6*8)+(5*1)+(4*9)+(3*4)+(2*5)+(1*5)=145
145 % 10 = 5
So 138194-55-5 is a valid CAS Registry Number.

138194-55-5SDS

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 3-maleimidopropionic acid pentafluorophenyl ester

1.2 Other means of identification

Product number -
Other names 3-(2,5-Dioxo-2,5-dihydro-pyrrol-1-yl)-propionic acid pentafluorophenyl ester

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:138194-55-5 SDS

138194-55-5Downstream Products

138194-55-5Relevant academic research and scientific papers

RNase P-Guiding Peptide Conjugates of Oligo(2'-O-methylribonucleotides) as Prospective Antibacterial Agents

Danilin,Koroleva,Novopashina,Venyaminova

, p. 825 - 832 (2019)

Abstract: A novel variant of the synthesis of 3'- and 5'-peptide conjugates of oligo(2'-O-methylribonucleotides) has been developed using thiol-maleimide chemistry. The method is based on the introduction of the maleimide group into an oligonucleotide usi

Facile synthesis of reagents containing a terminal maleimido ligand linked to an active ester

Nielsen,Buchardt

, p. 819 - 821 (2007/10/02)

Condensation of ω-amino acids with maleic anhydride to yield maleamino acids and subsequent esterification with N-hydroxysuccinimide, 3,4-dihydro-3-hydroxy-4-oxo-1,2,3-benzotriazine, or pentafluorophenol to give the corresponding esters in a one pot procedure are described. The reagents can be isolated and purified without chromatography in 7-55% yields.

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