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3-(2-hydroxypropan-2-yl)phenylboronic acid is a chemical compound with the molecular formula C9H13BO3. It is a boronic acid derivative characterized by a phenyl group attached to a boron atom through a carbon atom. 3-(2-hydroxypropan-2-yl)phenylboronic acid is known for its utility in various chemical processes and synthesis, making it a significant intermediate in organic chemistry.

955369-43-4

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955369-43-4 Usage

Uses

Used in Organic Synthesis:
3-(2-hydroxypropan-2-yl)phenylboronic acid is used as a building block for the synthesis of complex organic molecules. Its structural features allow it to serve as a versatile component in the creation of a wide range of chemical entities.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
In the field of organic chemistry, 3-(2-hydroxypropan-2-yl)phenylboronic acid is employed as a reagent in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful method for the formation of carbon-carbon bonds, which are crucial in the synthesis of many organic compounds, including pharmaceuticals and agrochemicals.
Used in Pharmaceutical Preparation:
3-(2-hydroxypropan-2-yl)phenylboronic acid is used as a precursor in the preparation of pharmaceuticals. The boronic acid functional group present in 3-(2-hydroxypropan-2-yl)phenylboronic acid is a key feature that enables the synthesis of biologically active compounds, which can be further developed into potential drug candidates.
Used in Agrochemical Development:
3-(2-hydroxypropan-2-yl)phenylboronic acid is also utilized in the development of agrochemicals, where its reactivity and structural properties are harnessed to create new molecules with pesticidal or herbicidal properties, contributing to the advancement of agricultural chemistry.
Used in Materials Science Applications:
3-(2-hydroxypropan-2-yl)phenylboronic acid is used as a component in the synthesis of new materials with potential applications in various industries. Its role in the development of novel materials is significant, as it can influence the properties of the final products, such as their stability, reactivity, or other functional characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 955369-43-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,5,3,6 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 955369-43:
(8*9)+(7*5)+(6*5)+(5*3)+(4*6)+(3*9)+(2*4)+(1*3)=214
214 % 10 = 4
So 955369-43-4 is a valid CAS Registry Number.
InChI:InChI=1S/C9H13BO3/c1-9(2,11)7-4-3-5-8(6-7)10(12)13/h3-6,11-13H,1-2H3

955369-43-4SDS

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 (3-(2-Hydroxypropan-2-yl)phenyl)boronic acid

1.2 Other means of identification

Product number -
Other names [3-(2-hydroxypropan-2-yl)phenyl]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:955369-43-4 SDS

955369-43-4Downstream Products

955369-43-4Relevant articles and documents

Dihydropyrazolopyrimidinone derivatives

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Page/Page column 42, (2008/06/13)

The invention relates to compounds of a general formula (I): wherein Ar1 is an optionally-substituted aryl or heteroaromatic group; R1 is an optionally-substituted lower alkyl, lower alkenyl, lower alkynyl or cyclo-lower alkyl group, or is an aryl, aralkyl or heteroaromatic group optionally having a substituent; R2 is a hydrogen atom, a lower alkyl group, a lower alkenyl group or a lower alkynyl group, or is an aryl, aralkyl or heteroaromatic group optionally having a substituent; R3 is a hydrogen atom or a lower alkyl group; R4 is a hydrogen atom, a halogen atom, a hydroxyl group, a lower alkyl group or a group of —N(R1k)R1m; T and U are a nitrogen atom or a methine group, etc. The compounds of the invention have excellent Weel kinase-inhibitory effect and are therefore useful in the field of medicines, especially treatment of various cancers.

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