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1035235-29-0

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1035235-29-0 Usage

General Description

4-Cyano-2-fluorobenzeneboronic acid, pinacol ester is a chemical compound with the formula C14H16BNO3. It is a boronic acid pinacol ester derivative, which means it contains a boronic acid functional group and a pinacol ester moiety. 4-Cyano-2-fluorobenzeneboronic acid, pinacol ester is commonly used in organic synthesis as a building block for the development of various pharmaceuticals, agrochemicals, and materials. It can also be utilized as a reagent in Suzuki-Miyaura coupling reactions to form carbon-carbon bonds, and in the synthesis of biaryl compounds. Additionally, it has potential applications in medicinal chemistry and drug discovery due to its ability to selectively modify biological targets with minimal side effects. Overall, 4-Cyano-2-fluorobenzeneboronic acid, pinacol ester is a versatile and valuable chemical compound in the field of organic and pharmaceutical chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1035235-29-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,5,2,3 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1035235-29:
(9*1)+(8*0)+(7*3)+(6*5)+(5*2)+(4*3)+(3*5)+(2*2)+(1*9)=110
110 % 10 = 0
So 1035235-29-0 is a valid CAS Registry Number.

1035235-29-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H59067)  4-Cyano-2-fluorobenzeneboronic acid pinacol ester, 96%   

  • 1035235-29-0

  • 250mg

  • 907.0CNY

  • Detail
  • Alfa Aesar

  • (H59067)  4-Cyano-2-fluorobenzeneboronic acid pinacol ester, 96%   

  • 1035235-29-0

  • 1g

  • 2906.0CNY

  • Detail

1035235-29-0SDS

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 3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile

1.2 Other means of identification

Product number -
Other names PC3223

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:1035235-29-0 SDS

1035235-29-0Relevant articles and documents

INHIBITORS OF RECEPTOR INTERACTING PROTEIN KINASE I FOR THE TREATMENT OF DISEASE

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Paragraph 0404, (2021/09/04)

Disclosed herein are compounds which inhibit RIPK1, pharmaceutical compositions, and methods of treatment of RIPK1-mediated diseases, such as neurodegenerative disorders, inflammatory disorders, and cancer.

ORGANIC ELECTROLUMINESCENCE DEVICE AND POLYCYCLIC COMPOUND FOR ORGANIC ELECTROLUMINESCENCE DEVICE

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Paragraph 0117; 0118, (2019/10/12)

An organic electroluminescence device includes a first electrode, a hole transport region disposed on the first electrode, an emission layer disposed on the hole transport region, an electron transport region disposed on the emission layer, and a second electrode disposed on the electron transport region, wherein the emission layer includes a polycyclic compound containing two electron donors and one electron acceptor, and the electron acceptor includes a benzonitrile part and a pyridine part, thereby showing high emission efficiency.

HETEROCYCLIC COMPOUND AND USE THEREOF

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Page/Page column 71, (2012/03/26)

The present invention provides a heterocycle derivative having a superior amyloid β production inhibitory activity and/or a superior γ-secretase modulation activity, and use thereof. A compound represented by the formula (I): wherein each symbol is as defined in the present specification, or a salt thereof.

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