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98139-72-1

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98139-72-1 Usage

Chemical Properties

solid

Uses

Reactant for:Selective copper-promoted cross-coupling with aromatic aminesSynthesis of indazole based analog sensitive Akt inhibitorsPreparation of alkylarenes via tetraphosphine-palladium-catalyzed Suzuki cross-coupling with aryl halides

Check Digit Verification of cas no

The CAS Registry Mumber 98139-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,1,3 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98139-72:
(7*9)+(6*8)+(5*1)+(4*3)+(3*9)+(2*7)+(1*2)=171
171 % 10 = 1
So 98139-72-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H13BO2/c1-5(2)3-4-6(7)8/h5,7-8H,3-4H2,1-2H3

98139-72-1 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (655090)  3-Methyl-1-butylboronicacid  

  • 98139-72-1

  • 655090-5G

  • 1,648.53CNY

  • Detail

98139-72-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Isopentylboronic acid

1.2 Other means of identification

Product number -
Other names 3-methylbutylboronic acid

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:98139-72-1 SDS

98139-72-1Relevant articles and documents

P1 Phenethyl peptide boronic acid inhibitors of HCV NS3 protease

Priestley,De Lucca, Indawati,Ghavimi, Bahman,Erickson-Viitanen, Susan,Decicco, Carl P.

, p. 3199 - 3202 (2007/10/03)

A series of peptide boronic acids containing extended, hydrophobic P1 residues was prepared to probe the shallow, hydrophobic S1 region of HCV NS3 protease. The p-trifluoromethylphenethyl P1 substituent was identified as optimal with respect to inhibitor potency for NS3 and selectivity against elastase and chymotrypsin.

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