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486422-68-8

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486422-68-8 Usage

General Description

"4-(Morpholinosulfonyl)phenylboronic acid" is a chemical compound that primarily functions as a reagent used in laboratory settings. It has a molecular weight of 261.056g/mol and is typically available as a white solid. The reactions involving this compound are typically done under mild conditions, making it a popular choice for various molecular transformations. Furthermore, "4-(Morpholinosulfonyl)phenylboronic acid" plays a role in Suzuki-Miyaura coupling reactions, which are commonly used for constructing carbon-carbon bonds. It's noteworthy for its stability and substrate versatility during these reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 486422-68-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,6,4,2 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 486422-68:
(8*4)+(7*8)+(6*6)+(5*4)+(4*2)+(3*2)+(2*6)+(1*8)=178
178 % 10 = 8
So 486422-68-8 is a valid CAS Registry Number.

486422-68-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-morpholin-4-ylsulfonylphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 4-(morpholine-4-sulfonyl)-phenylboronic 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:486422-68-8 SDS

486422-68-8Relevant articles and documents

Antiparasitic Lead Discovery: Toward Optimization of a Chemotype with Activity Against Multiple Protozoan Parasites

Devine, William,Thomas, Sarah M.,Erath, Jessey,Bachovchin, Kelly A.,Lee, Patricia J.,Leed, Susan E.,Rodriguez, Ana,Sciotti, Richard J.,Mensa-Wilmot, Kojo,Pollastri, Michael P.

, p. 350 - 354 (2017/03/17)

Human African trypanosomiasis (HAT), Chagas disease, and leishmaniasis present a significant burden across the developing world. Existing therapeutics for these protozoal neglected tropical diseases suffer from severe side effects and toxicity. Previously

Discovery of a potent CDK2 inhibitor with a novel binding mode, using virtual screening and initial, structure-guided lead scoping

Richardson, Christine M.,Nunns, Claire L.,Williamson, Douglas S.,Parratt, Martin J.,Dokurno, Pawel,Howes, Rob,Borgognoni, Jenifer,Drysdale, Martin J.,Finch, Harry,Hubbard, Roderick E.,Jackson, Philip S.,Kierstan, Peter,Lentzen, Georg,Moore, Jonathan D.,Murray, James B.,Simmonite, Heather,Surgenor, Allan E.,Torrance, Christopher J.

, p. 3880 - 3885 (2008/02/08)

Virtual screening against a pCDK2/cyclin A crystal structure led to the identification of a potent and novel CDK2 inhibitor, which exhibited an unusual mode of interaction with the kinase binding motif. With the aid of X-ray crystallography and modelling,

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