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4-Chloro-3-trifluoromethylphenylboronic acid, pinacol ester is a boronic acid-derived reagent used in organic synthesis. It serves as a source of the phenyltrifluoroborate functional group, which is valuable in pharmaceutical and agrochemical industries. This chemical compound is stable, easy to handle, and offers a unique combination of reactivity and stability, making it a versatile tool for constructing complex molecular architectures and a valuable building block for the synthesis of diverse biologically active compounds.

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  • 445303-09-3 Structure
  • Basic information

    1. Product Name: 4-CHLORO-3-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER
    2. Synonyms: 2-[4-Chloro-3-(trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzotrifluoride;2-(4-chloro-3-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;4-CHLORO-3-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER;4-Chloro-3-trifluoromethylphenylboronic acid,pinacol;1,3,2-Dioxaborolane, 2-[4-chloro-3-(trifluoroMethyl)phenyl]-4,4,5,5-tetraMethyl-
    3. CAS NO:445303-09-3
    4. Molecular Formula: C13H15BClF3O2
    5. Molecular Weight: 306.52
    6. EINECS: N/A
    7. Product Categories: Aryl;Organoborons;Trifluoromethyl
    8. Mol File: 445303-09-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 327.076°C at 760 mmHg
    3. Flash Point: 151.611°C
    4. Appearance: /
    5. Density: 1.237g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.471
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-CHLORO-3-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-CHLORO-3-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER(445303-09-3)
    12. EPA Substance Registry System: 4-CHLORO-3-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER(445303-09-3)
  • Safety Data

    1. Hazard Codes: Xi,Xn
    2. Statements: 22
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 445303-09-3(Hazardous Substances Data)

445303-09-3 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-3-trifluoromethylphenylboronic acid, pinacol ester is used as a reagent in cross-coupling reactions for the synthesis of pharmaceutical compounds. Its phenyltrifluoroborate functional group contributes to the development of complex molecular architectures, enabling the creation of diverse biologically active compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 4-chloro-3-trifluoromethylphenylboronic acid, pinacol ester is utilized as a reagent for the synthesis of agrochemical compounds. Its unique functional group aids in the development of complex molecular structures, which can be used to create effective and targeted agrochemical products for crop protection and other agricultural applications.
Used in Organic Synthesis:
4-Chloro-3-trifluoromethylphenylboronic acid, pinacol ester is employed as a versatile reagent in organic synthesis for the construction of complex molecular architectures. Its stability and ease of handling make it an ideal building block for the synthesis of a wide range of biologically active compounds, contributing to the advancement of chemical research and development.

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.

Imidazole derivatives

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, (2008/06/13)

Novel imidazole derivatives are disclosed. These compounds have a good affinity to the NMDA (N-methyl-D-aspartate)-receptor subtype selective blockers, which have a key function in modulating neuronal activity and plasticity which makes them key players in mediating processes underlying development of CNS as well as learning and memory formation. These compounds are useful in the control or treatment of diseases mediated by this receptor.

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