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N,N-Dimethyl 4-borono-3-methylbenzenesulfonamide is a versatile chemical compound utilized in various organic synthesis processes. It features a boron atom connected to a benzene ring, which is adorned with a sulfonamide group and two methyl groups. N,N-Dimethyl 4-borono-3-methylbenzenesulfonamide is recognized for its Lewis acid properties, particularly in facilitating Suzuki-Miyaura cross-coupling reactions, a significant method in the formation of carbon-carbon bonds. Moreover, its applications extend to the synthesis of pharmaceuticals and fine chemicals, capitalizing on its reactivity and structural attributes. The presence of a boron atom also positions N,N-Dimethyl 4-borono-3-methylbenzenesulfonamide as a candidate for boron neutron capture therapy, a targeted radiation treatment for cancer.

957034-82-1

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957034-82-1 Usage

Uses

Used in Organic Synthesis:
N,N-Dimethyl 4-borono-3-methylbenzenesulfonamide is used as a Lewis acid catalyst for facilitating Suzuki-Miyaura cross-coupling reactions, which are crucial for the formation of carbon-carbon bonds in organic molecules. Its ability to act as a Lewis acid enhances the reactivity and selectivity of these reactions, making it a valuable component in the synthesis of complex organic compounds.
Used in Pharmaceutical and Fine Chemicals Synthesis:
In the pharmaceutical industry, N,N-Dimethyl 4-borono-3-methylbenzenesulfonamide serves as a reagent in the synthesis of various drugs and fine chemicals. Its unique structure and reactivity contribute to the creation of novel compounds with potential therapeutic applications.
Used in Cancer Treatment Research:
N,N-Dimethyl 4-borono-3-methylbenzenesulfonamide is studied for its potential use in boron neutron capture therapy, a targeted radiation treatment for cancer. The boron atom in the compound can be selectively taken up by tumor cells, and when exposed to neutron radiation, it can generate cytotoxic effects, selectively destroying cancer cells while minimizing damage to surrounding healthy tissue. This research is ongoing and aims to explore the therapeutic potential of N,N-Dimethyl 4-borono-3-methylbenzenesulfonamide in cancer treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 957034-82-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,0,3 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 957034-82:
(8*9)+(7*5)+(6*7)+(5*0)+(4*3)+(3*4)+(2*8)+(1*2)=191
191 % 10 = 1
So 957034-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H14BNO4S/c1-7-6-8(16(14,15)11(2)3)4-5-9(7)10(12)13/h4-6,12-13H,1-3H3

957034-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-(N,N-Dimethylsulfamoyl)-2-methylphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names [4-(dimethylsulfamoyl)-2-methylphenyl]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:957034-82-1 SDS

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