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4-(ISOPROPYLSULFONYLPHENYL)BORONIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

850567-98-5

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850567-98-5 Usage

Uses

4-Isopropylsulfonylphenylboronic acid

Check Digit Verification of cas no

The CAS Registry Mumber 850567-98-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,5,6 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 850567-98:
(8*8)+(7*5)+(6*0)+(5*5)+(4*6)+(3*7)+(2*9)+(1*8)=195
195 % 10 = 5
So 850567-98-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H13BO4S/c1-7(2)15(13,14)9-5-3-8(4-6-9)10(11)12/h3-7,11-12H,1-2H3

850567-98-5SDS

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 4-Isopropylsulfonylbenzeneboronic acid

1.2 Other means of identification

Product number -
Other names (4-propan-2-ylsulfonylphenyl)boronic 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:850567-98-5 SDS

850567-98-5Relevant academic research and scientific papers

Preparation method of 4-isopropylsulfonylphenylboronic acid

-

, (2021/04/26)

The invention discloses a preparation method of 4-isopropylsulfonylphenylboronic acid, and belongs to the technical field of organic synthesis. The preparation method comprises the following steps of: taking 4-bromothiophenol and halogenated isopropane as the raw materials, and acquiring 1-bromo-4-isopropyl thiobenzene under the action of potassium carbonate; performing oxidizing with hydrogen peroxide in the presence of a catalyst to obtain 1-bromo-4-isopropylsulfonylbenzene, and finally, carrying out Grignard exchange/borate reaction with a Grignard reagent to obtain 4-isopropylsulfonylphenylboronic acid. The method has the advantages of high yield, simple process, cheap and easily available raw materials, green chemistry, and 6 times of application of the catalyst, and has an industrial amplification prospect.

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