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(3-ethoxy-4-Methylphenyl)boronic acid is a white solid chemical compound that belongs to the boronic acid family. It features a boronic acid group attached to a phenyl ring with an ethoxy and methyl substituent, which contributes to its versatility in forming various chemical bonds. (3-ethoxy-4-Methylphenyl)boronic acid is typically used as a reagent in organic synthesis and medicinal chemistry, known for its ability to react with a variety of organic molecules.

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  • 1451391-68-6 Structure
  • Basic information

    1. Product Name: (3-ethoxy-4-Methylphenyl)boronic acid
    2. Synonyms: (3-ethoxy-4-Methylphenyl)boronic acid
    3. CAS NO:1451391-68-6
    4. Molecular Formula: C9H13BO3
    5. Molecular Weight: 180.00872
    6. EINECS: N/A
    7. Product Categories: Boronate Ester;Boronic Acid;Potassium Trifluoroborate
    8. Mol File: 1451391-68-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: (3-ethoxy-4-Methylphenyl)boronic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-ethoxy-4-Methylphenyl)boronic acid(1451391-68-6)
    11. EPA Substance Registry System: (3-ethoxy-4-Methylphenyl)boronic acid(1451391-68-6)
  • 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: 1451391-68-6(Hazardous Substances Data)

1451391-68-6 Usage

Uses

Used in Organic Synthesis:
(3-ethoxy-4-Methylphenyl)boronic acid is used as a reagent for the formation of carbon-carbon and carbon-oxygen bonds in the synthesis of complex molecules. Its ability to react with a variety of organic molecules makes it a valuable component in creating intricate molecular structures.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (3-ethoxy-4-Methylphenyl)boronic acid is utilized in the development of pharmaceuticals. Its versatility in forming chemical bonds allows for the creation of diverse drug candidates with potential therapeutic applications.
Used in Agrochemical Development:
(3-ethoxy-4-Methylphenyl)boronic acid is also employed in the development of agrochemicals, where its reactivity and bond-forming capabilities contribute to the synthesis of compounds with pesticidal or herbicidal properties.
Used in Materials Science:
In the field of materials science, (3-ethoxy-4-Methylphenyl)boronic acid is used for the synthesis of new materials with specific properties. Its ability to form various chemical bonds can lead to the development of materials with unique characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1451391-68-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,1,3,9 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1451391-68:
(9*1)+(8*4)+(7*5)+(6*1)+(5*3)+(4*9)+(3*1)+(2*6)+(1*8)=156
156 % 10 = 6
So 1451391-68-6 is a valid CAS Registry Number.

1451391-68-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Boronic acid, B-?(3-?ethoxy-?4-?methylphenyl)?-

1.2 Other means of identification

Product number -
Other names -

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:1451391-68-6 SDS

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