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Boronic acid, [3-[(butylmethylamino)sulfonyl]phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

690662-94-3

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690662-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 690662-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,0,6,6 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 690662-94:
(8*6)+(7*9)+(6*0)+(5*6)+(4*6)+(3*2)+(2*9)+(1*4)=193
193 % 10 = 3
So 690662-94-3 is a valid CAS Registry Number.

690662-94-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-[butyl(methyl)sulfamoyl]phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names -

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:690662-94-3 SDS

690662-94-3Downstream Products

690662-94-3Relevant academic research and scientific papers

Structure-activity relationship for aryl and heteroaryl boronic acid inhibitors of hormone-sensitive lipase

Ebdrup, Soren,Jacobsen, Poul,Farrington, Anupma Dhanda,Vedso, Per

, p. 2305 - 2312 (2007/10/03)

A range of aryl and heteroaryl boronic acids were tested for their in vitro hormone-sensitive lipase inhibitory properties. (2-Benzyloxy-5-fluorophenyl) boronic acid, (2-benzyloxy-5-chlorophenyl)boronic acid and 5-bromothiophene-2- boronic acid were found to be the most potent HSL inhibitors with IC 50 values of 140, 17 and 350 nM, respectively.

Synthesis of sulfonyl chlorides of phenylboronic acids

Veds?, Per,Olesen, Preben H.,Hoeg-Jensen, Thomas

, p. 892 - 894 (2007/10/03)

Sulfonyl chlorides of phenylboronic esters have been made available by selective lithiation of bromo N-methyl-diethanolamine phenylboronates to give lithium sulfinyl phenylboronates as intermediates. Oxidations with N-chlorosuccinimide give the target sul

HALO SULFONYL ARYL BORONATES

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Page 12, (2010/02/07)

The present invention relates to halo sulfonyl aryl boronates of the general formula (I): wherein Arylene designates a carbocyclic or heterocyclic, aromatic ring system comprising 1-3 rings; R1, R2 and R3 are, independently, hydrogen, C1-6alkyl, C1-6alkoxy, halogen, nitro, cyano or phenyl;X is fluoro, chloro or bromo; and Y is a boroxine moiety attached via a bond from Arylene to one of the boron atoms of a boroxine ring which ring has a group of the formula -Arylene(R1)(R2)(R3)SO2X, wherein Arylene, R1, R2, R3 and X are as defined above, at each of the other two boron atoms of the boroxine ring, or Y is a boronic acid group or a boronic ester group.The invention also relates to the preparation of the compounds of formula (I) and to their use in organic synthesis.

Halo sulfonyl aryl boronates

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Page 6, (2010/02/07)

The present invention relates to halo sulfonyl aryl boronates of the general formula (I): wherein Arylene designates a carbocyclic or heterocyclic, aromatic ring system comprising 1-3 rings; R1, R2 and R3 are, independentl

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