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3,5-Difluoro-4-carboxyphenylboronic acid is an organic compound and a derivative of boronic acid. It is characterized by the presence of a boronic acid group, which allows it to form covalent bonds with other compounds, making it a valuable asset in specialized synthesis in organic chemistry. The fluorine substitutions on the phenyl ring enhance its electron-withdrawing properties, increasing the chemical's overall reactivity. Furthermore, the carboxy functional group enables this compound to participate in carboxylation reactions. Due to its unique physical and chemical properties, 3,5-Difluoro-4-carboxyphenylboronic acid plays a crucial part in organic synthesis.

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  • 1029716-94-6 Structure
  • Basic information

    1. Product Name: 3,5-Difluoro-4-carboxyphenylboronic acid
    2. Synonyms: 3,5-Difluoro-4-carboxyphenylboronic acid;4-Borono-2,6-difluorobenzoic acid
    3. CAS NO:1029716-94-6
    4. Molecular Formula: C7H5BF2O4
    5. Molecular Weight: 201.9200064
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1029716-94-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 383.8±52.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.58±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 2.22±0.10(Predicted)
    10. CAS DataBase Reference: 3,5-Difluoro-4-carboxyphenylboronic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3,5-Difluoro-4-carboxyphenylboronic acid(1029716-94-6)
    12. EPA Substance Registry System: 3,5-Difluoro-4-carboxyphenylboronic acid(1029716-94-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1029716-94-6(Hazardous Substances Data)

1029716-94-6 Usage

Uses

Used in Organic Synthesis:
3,5-Difluoro-4-carboxyphenylboronic acid is used as a synthetic intermediate for the preparation of various chemical and pharmaceutical products. Its boronic acid group facilitates the formation of covalent bonds with other compounds, making it a versatile building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
3,5-Difluoro-4-carboxyphenylboronic acid is used as a key component in the development of new drugs. Its unique reactivity and the ability to participate in carboxylation reactions make it a valuable tool in the design and synthesis of novel pharmaceutical agents.
Used in Material Science:
3,5-Difluoro-4-carboxyphenylboronic acid is used as a functional group in the creation of new materials with specific properties. The electron-withdrawing nature of the fluorine substitutions and the carboxy functional group contribute to the development of materials with tailored characteristics for various applications in material science.

Check Digit Verification of cas no

The CAS Registry Mumber 1029716-94-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,9,7,1 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1029716-94:
(9*1)+(8*0)+(7*2)+(6*9)+(5*7)+(4*1)+(3*6)+(2*9)+(1*4)=156
156 % 10 = 6
So 1029716-94-6 is a valid CAS Registry Number.

1029716-94-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Borono-2,6-difluorobenzoic acid

1.2 Other means of identification

Product number -
Other names 4-borono-2,6-difluorobenzoic 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:1029716-94-6 SDS

1029716-94-6Downstream Products

1029716-94-6Relevant articles and documents

Ortho-substituted aryl monoboronic acids have improved selectivity for d-glucose relative to d-fructose and l-lactate

Hansen,Christensen,Solling,Jakobsen,Hoeg-Jensen

, p. 1334 - 1340 (2011)

Ortho-substituted aryl monoboronic acids have been found to have improved selectivity for d-glucose compared to d-fructose and l-lactate. These findings are supported by computational studies on the B3LYP/6-31G(d) level using Gaussian. This finding is of

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