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Benzenemethanol, 2-(methylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- is a complex organic compound with the molecular formula C14H23BO4S. It is a derivative of benzenemethanol, featuring a methylsulfonyl group at the 2-position and a 1,3,2-dioxaborolane group at the 4-position. Benzenemethanol, 2-(methylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- is significant in organic synthesis, particularly in cross-coupling reactions, due to the presence of the boron-containing dioxaborolane moiety. It serves as a precursor in the synthesis of various pharmaceuticals and agrochemicals, where its reactivity and selectivity are harnessed to form carbon-carbon bonds. The compound's structure allows for the introduction of functional groups at specific positions on the benzene ring, which is crucial for the development of targeted molecular structures with desired properties.

918328-16-2

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918328-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918328-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,3,2 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 918328-16:
(8*9)+(7*1)+(6*8)+(5*3)+(4*2)+(3*8)+(2*1)+(1*6)=182
182 % 10 = 2
So 918328-16-2 is a valid CAS Registry Number.

918328-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-(methylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol

1.2 Other means of identification

Product number -
Other names [2-methanesulfonyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanol

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:918328-16-2 SDS

918328-16-2Relevant academic research and scientific papers

Discovery of Highly Potent Liver X Receptor β Agonists

Kick, Ellen K.,Busch, Brett B.,Martin, Richard,Stevens, William C.,Bollu, Venkataiah,Xie, Yinong,Boren, Brant C.,Nyman, Michael C.,Nanao, Max H.,Nguyen, Lam,Plonowski, Artur,Schulman, Ira G.,Yan, Grace,Zhang, Huiping,Hou, Xiaoping,Valente, Meriah N.,Narayanan, Rangaraj,Behnia, Kamelia,Rodrigues, A. David,Brock, Barry,Smalley, James,Cantor, Glenn H.,Lupisella, John,Sleph, Paul,Grimm, Denise,Ostrowski, Jacek,Wexler, Ruth R.,Kirchgessner, Todd,Mohan, Raju

, p. 1207 - 1212 (2016/12/18)

Introducing a uniquely substituted phenyl sulfone into a series of biphenyl imidazole liver X receptor (LXR) agonists afforded a dramatic potency improvement for induction of ATP binding cassette transporters, ABCA1 and ABCG1, in human whole blood. The ag

LIVER X RECEPTOR (LXR) MODULATORS

-

, (2015/03/28)

Described herein are liver X receptor (LXR) modulators and methods of utilizing LXR modulators in the treatment of dermal diseases, disorders or conditions. Also described herein are pharmaceutical compositions containing such compounds.

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