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2-(2,3-DIHYDROBENZOFURAN-6-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE is a boron-containing organic compound that serves as a versatile reagent in Suzuki-Miyaura cross-coupling reactions. It is characterized by its stability, selectivity, and unique structure, which allows it to form strong carbon-carbon bonds with a variety of organic substrates. 2-(2,3-DIHYDROBENZOFURAN-6-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE is highly valued in the synthesis of new pharmaceuticals, agrochemicals, and advanced materials, as well as in the development of materials for electronic and optoelectronic applications.

445303-12-8

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  • 2-(2,3-dihydrobenzofuran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

    Cas No: 445303-12-8

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445303-12-8 Usage

Uses

Used in Pharmaceutical Synthesis:
2-(2,3-DIHYDROBENZOFURAN-6-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE is used as a reagent in the synthesis of pharmaceuticals for its ability to create carbon-carbon bonds, which are essential in the development of new drug molecules.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2-(2,3-DIHYDROBENZOFURAN-6-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE is used as a reagent to form carbon-carbon bonds in the synthesis of new agrochemical compounds, contributing to the development of effective and environmentally friendly pesticides and fertilizers.
Used in Advanced Material Synthesis:
2-(2,3-DIHYDROBENZOFURAN-6-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE is utilized as a reagent in the synthesis of advanced materials, where its ability to form stable and selective carbon-carbon bonds is crucial for creating innovative materials with enhanced properties.
Used in Electronic and Optoelectronic Material Development:
In the field of electronics and optoelectronics, 2-(2,3-DIHYDROBENZOFURAN-6-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE is used as a component in the development of new materials, leveraging its boron functionality to create materials with improved electronic and optoelectronic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 445303-12-8 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, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 445303-12:
(8*4)+(7*4)+(6*5)+(5*3)+(4*0)+(3*3)+(2*1)+(1*2)=118
118 % 10 = 8
So 445303-12-8 is a valid CAS Registry Number.

445303-12-8SDS

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-(2,3-dihydro-1-benzofuran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names COUMARAN-6-BORONIC ACID PINACOL ESTER

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:445303-12-8 SDS

445303-12-8Downstream Products

445303-12-8Relevant articles and documents

PYRIMIDINE SULFAMIDE DERIVATIVE AND PREPARATION METHOD AND MEDICAL APPLICATION THEREOF

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Paragraph 0315; 0318-0319, (2020/09/22)

Disclosed are a series of pyrimidine sulfamide compounds and applications thereof in preparing a drug for a disease related to an ETA receptor antagonist. In particular, disclosed is a derived compound represented by formula (I) or a tautomer or pharmaceutically acceptable composition thereof.

Condensed derivatives of imidazole useful as pharmaceuticals

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Paragraph 0446; 0722, (2015/09/23)

The invention relates to the compounds (I) and their acids and bases salts: wherein: the dotted line indicates a double bond; X is N or C-R1 and Y is N or C-R2, X and Y not being simultaneously N; A is selected from the group consisting of phenyl, naphthyl and (5-11) membered monocyclic or bicyclic unsaturated cycle or heterocycle possibly substituted as defined in the application, and A can also comprise either a further (4-7) membered heterocycle, said heterocycle being a monocycle, fused, saturated or unsaturated, the polycyclic system then comprising up to 14 members and up to 5 heteroatoms selected from N, O and S; B is Hydrogen or a substituent as defined in the application, or B is a (4-10) membered mono or bicyclic saturated or unsaturated heterocycle containing 1-3 heteroatoms selected from N, O and S, and possibly substituted as defined in the application; B not being Hydrogen when X is N and Y is C-R2; R1 is Hydrogen or a substituent as defined in the application; B and R1 cannot be simultaneously Hydrogen; R2 is Hydrogen or Halogen; their preparation, their use in the antibacterial prevention and therapy, alone or in association with antibacterials, antivirulence agents or drugs reinforcing the host innate immunity, and pharmaceutical compositions and associations containing them.

NEW COMPOUNDS

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Page/Page column 83, (2008/06/13)

This invention relates to novel compounds having the structural formula I below: and to their pharmaceutically acceptable salt, compositions and methods of use. These novel compounds provide a treatment or prophylaxis of cognitive impairment, Alzheimer Disease, neurodegeneration and dementia.

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