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135145-90-3

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135145-90-3 Usage

Description

2,5-Dichlorophenylboronic acid is an organic compound with the chemical formula C6H4Cl2BO2H. It is a white to off-white powder and is commonly used as a reactant in various chemical reactions and synthesis processes. Its chemical structure features a boronic acid group attached to a dichloro-substituted benzene ring, which allows it to participate in a range of chemical reactions.

Uses

1. Used in Pharmaceutical Industry:
2,5-Dichlorophenylboronic acid is used as a reactant for the synthesis of Dipeptidyl peptidase IV (DPP4) inhibitors, which are crucial in the treatment of type 2 diabetes. These inhibitors help regulate blood sugar levels by slowing down the degradation of certain hormones.
2. Used in Chemical Synthesis:
2,5-Dichlorophenylboronic acid is used as a reactant in various chemical reactions, such as:
a. Regioselective iodination using silver salts, which allows for the selective introduction of iodine atoms into specific positions on the molecule.
b. Pd-catalyzed Suzuki-Miyaura coupling, a widely used method for the formation of carbon-carbon bonds, particularly in the synthesis of complex organic molecules.
c. Rhodium(I)-catalyzed carbonylative cyclization of alkynes, a reaction that involves the formation of cyclic compounds with a carbonyl group.
d. Copper-catalyzed coupling reactions, which are employed in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 135145-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,1,4 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 135145-90:
(8*1)+(7*3)+(6*5)+(5*1)+(4*4)+(3*5)+(2*9)+(1*0)=113
113 % 10 = 3
So 135145-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BCl2O2/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,10-11H

135145-90-3 Well-known Company Product Price

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  • TCI America

  • (D3044)  2,5-Dichlorophenylboronic Acid (contains varying amounts of Anhydride)  

  • 135145-90-3

  • 5g

  • 580.00CNY

  • Detail
  • TCI America

  • (D3044)  2,5-Dichlorophenylboronic Acid (contains varying amounts of Anhydride)  

  • 135145-90-3

  • 25g

  • 2,250.00CNY

  • Detail
  • Alfa Aesar

  • (B22984)  2,5-Dichlorobenzeneboronic acid, 98%   

  • 135145-90-3

  • 1g

  • 455.0CNY

  • Detail
  • Alfa Aesar

  • (B22984)  2,5-Dichlorobenzeneboronic acid, 98%   

  • 135145-90-3

  • 5g

  • 1425.0CNY

  • Detail
  • Alfa Aesar

  • (B22984)  2,5-Dichlorobenzeneboronic acid, 98%   

  • 135145-90-3

  • 25g

  • 6437.0CNY

  • Detail

135145-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-Dichlorophenylboronic acid

1.2 Other means of identification

Product number -
Other names 2,5-Dichlorophenylbo

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:135145-90-3 SDS

135145-90-3Upstream product

135145-90-3Relevant articles and documents

Pyrazine compounds

-

, (2008/06/13)

A compound of formula (I) wherein R1is selected from the group consisting of phenyl substituted by one or more halogen atoms, naphthyl and naphthyl substituted by one or more halogen atoms; R2is selected from the group consisting of —NH2and —NHC(═O)Ra; R3is selected from the group consisting of —NRbRc, —NHC(═O)Raand hydrogen, R4is selected from the group consisting of hydrogen, -C1-4alkyl, -C1-4alkyl substituted by one or more halogen atoms, —CN, —CH2OH, —CH2ORdand —CH2S(O)xRd; wherein Rarepresents C1-4alkyl or C3-7cycloalkyl, and Rband Rc, which may be the same or different, are selected from hydrogen and C1-4alkyl, or together with the nitrogen atom to which they are attached, form a6-membered nitrogen containing heterocycle, which heterocycle can be further susbtituted with one or more C1-4alkyl; Rdis selected from C1-4alkyl or C1-4alkyl substituted by one or more halogen atoms; x is an integer zero, one or two; and pharmaceutically acceptable derivatives thereof; with the proviso that R1does not represent (a); when R2is —NH2, and both R3and R4are hydrogen.

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