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3-Cyano-5-fluorobenzeneboronic acid pinacol ester, 96% is a high-purity boronic acid derivative that serves as a versatile building block in organic synthesis and pharmaceutical research. Its high purity level of 96% makes it a reliable and effective reagent for researchers and scientists in the field of organic chemistry.

935685-88-4

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935685-88-4 Usage

Uses

Used in Organic Synthesis:
3-Cyano-5-fluorobenzeneboronic acid pinacol ester, 96% is used as a versatile building block for the synthesis of various organic molecules. Its unique structure allows for the creation of a wide range of compounds, making it a valuable tool in the development of new organic materials.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-Cyano-5-fluorobenzeneboronic acid pinacol ester, 96% is used as a key intermediate in the synthesis of various pharmaceuticals. Its high purity and reactivity make it an ideal candidate for the development of new drugs and therapeutic agents.
Used in Agrochemical Development:
3-Cyano-5-fluorobenzeneboronic acid pinacol ester, 96% is also utilized in the agrochemical industry for the synthesis of various agrochemicals. Its ability to form a wide range of compounds makes it a valuable resource for the development of new pesticides, herbicides, and other agricultural chemicals.
Used in Laboratory and Industrial Settings:
Due to its high purity and effectiveness, 3-Cyano-5-fluorobenzeneboronic acid pinacol ester, 96% is a reliable reagent for use in both laboratory and industrial settings. Its versatility and reactivity make it suitable for a wide range of applications, from research and development to large-scale production processes.

Check Digit Verification of cas no

The CAS Registry Mumber 935685-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,5,6,8 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 935685-88:
(8*9)+(7*3)+(6*5)+(5*6)+(4*8)+(3*5)+(2*8)+(1*8)=224
224 % 10 = 4
So 935685-88-4 is a valid CAS Registry Number.

935685-88-4 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H62066)  3-Cyano-5-fluorobenzeneboronic acid pinacol ester, 96%   

  • 935685-88-4

  • 250mg

  • 1386.0CNY

  • Detail
  • Alfa Aesar

  • (H62066)  3-Cyano-5-fluorobenzeneboronic acid pinacol ester, 96%   

  • 935685-88-4

  • 1g

  • 4158.0CNY

  • Detail

935685-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

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

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:935685-88-4 SDS

935685-88-4Relevant academic research and scientific papers

1,3-THIAZOL-2-YL SUBSTITUTED BENZAMIDES

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Page/Page column 206; 207, (2016/07/05)

The present invention relates to 1,3-thiazol-2-yl substituted benzamide compounds of general formula (I) as described and defined herein, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of neurogenic disorder, as a sole agent or in combination with other active ingredients.

INDOLIZINE DERIVATIVES AS PHOSHOINOSITIDE 3-KINASES INHIBITORS

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Paragraph 0785; 0786, (2015/12/31)

Compounds of formula (I), defined herein, inhibit phosphoinositide 3-kinases (PI3K) and are useful for the treatment of disorders associated with PI3K enzymes.

SUBSTITUTED (THIAZOLYL-CARBONYL)IMIDAZOLIDINONES AND USE THEREOF

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Paragraph 0224; 0225; 0226; 0227, (2013/03/26)

The present invention relates to novel substituted furancarboxamides, methods for their production, their use for the treatment and/or prevention of diseases, as well as their use for the production of medicaments for the treatment and/or prophylaxis of diseases, especially retroviral diseases, in humans and/or animals.

SUBSTITUTED (THIOPHENYL-CARBONYL)IMIDAZOLIDINONES, AND USE THEREOF

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Page/Page column 12, (2012/02/03)

The present invention relates to novel substituted (thiophenyl-carbonyl)imidazolidinones, methods for their production, their use for the treatment and/or prevention of diseases, as well as their use for the production of medicaments for the treatment and/or prophylaxis of diseases, especially retroviral diseases, in humans and/or animals.

SUBSTITUTED FURANCARBOXAMIDES, AND USE THEREOF

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Page/Page column 11, (2012/02/03)

The present invention relates to novel substituted furancarboxamides, methods for their production, their use for the treatment and/or prevention of diseases, as well as their use for the production of medicaments for the treatment and/or prophylaxis of diseases, especially retroviral diseases, in humans and/or animals.

BIARYL OXYACETIC ACID COMPOUNDS

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Page/Page column 52, (2010/09/18)

The present invention provides biaryl oxyacetic acid compounds which may be useful for treating inflammatory disorders, including disorders affecting the respiratory system and skin. The compounds provided include those of the general formula I.

Thiazolyl mglur5 antagonists and methods for their use

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Page/Page column 9, (2009/08/18)

The identification of a unique series of compounds which possesses special advantages in terms of drug-like properties due to their possessing advantageous properties in terms of potency and/or pharmacokinetic and/or selectivity and/or in vivo receptor occupancy properties. Specifically, the selection of a 1,3-thiazol-2-yl ring member linked by an ethynylene to the 3 position of a pyridyl ring or the 5 position of a pyrimidinyl ring, wherein the ring is substituted with selected substituents, results in a compound having superior drug-like properties. The invention includes pharmaceutically acceptable salt forms of these heterocyclic compounds, in particular chloride salts and trifluoroacetate salts.

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