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445303-09-3

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445303-09-3 Usage

General Description

4-Chloro-3-trifluoromethylphenylboronic acid, pinacol ester is a chemical compound used in organic synthesis as a reagent for cross-coupling reactions with various organic substrates. It is a boronic acid-derived reagent that serves as a source of the phenyltrifluoroborate functional group, which is valuable in pharmaceutical and agrochemical industries. 4-CHLORO-3-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER is stable and easy to handle, making it a versatile tool for the construction of complex molecular architectures. Its unique combination of reactivity and stability makes it a valuable building block for the synthesis of diverse biologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 445303-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,5,3,0 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 445303-09:
(8*4)+(7*4)+(6*5)+(5*3)+(4*0)+(3*3)+(2*0)+(1*9)=123
123 % 10 = 3
So 445303-09-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H15BClF3O2/c1-11(2)12(3,4)20-14(19-11)8-5-6-10(15)9(7-8)13(16,17)18/h5-7H,1-4H3

445303-09-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-chloro-3-(trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzotrifluoride

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:445303-09-3 SDS

445303-09-3Relevant articles and documents

Substituted imidazol-pyridazine derivatives

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Page 17, (2010/02/05)

The present invention relates to compounds of formula wherein A is an unsubstituted or substituted cyclic group; and R is hydrogen or lower alkyl; or a pharmaceutically acceptable acid addition salt thereof. These compounds are NMDA NR-2B receptor subtype specific blockers and are useful in the treatment of neurodegeneration, depression and pain.

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