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2-(Hydroxymethyl)-6-methoxyphenylboronic acid dehydrate is a boronic acid derivative with the molecular formula C8H13BO4. It features a phenyl ring with a hydroxymethyl and a methoxy group attached, along with a boronic acid functional group. The dehydrate form suggests the presence of water molecules within its structure. This versatile chemical is widely utilized in various applications due to its unique reactivity and properties.

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  • 947163-27-1 Structure
  • Basic information

    1. Product Name: 2-(Hydroxymethyl)-6-methoxyphenylboronic acid dehydrate
    2. Synonyms: 2-(Hydroxymethyl)-6-methoxyphenylboronic acid dehydrate;7-Methoxybenzo[c][1,2]oxaborol-1(3H)-ol
    3. CAS NO:947163-27-1
    4. Molecular Formula: C8H9BO3
    5. Molecular Weight: 163.97
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 947163-27-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 300.5±52.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.21±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Room temperature.
    8. Solubility: N/A
    9. PKA: 7.14±0.20(Predicted)
    10. CAS DataBase Reference: 2-(Hydroxymethyl)-6-methoxyphenylboronic acid dehydrate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(Hydroxymethyl)-6-methoxyphenylboronic acid dehydrate(947163-27-1)
    12. EPA Substance Registry System: 2-(Hydroxymethyl)-6-methoxyphenylboronic acid dehydrate(947163-27-1)
  • 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: 947163-27-1(Hazardous Substances Data)

947163-27-1 Usage

Uses

Used in Organic Synthesis:
2-(Hydroxymethyl)-6-methoxyphenylboronic acid dehydrate is used as a reagent in the Suzuki-Miyaura cross-coupling reaction, a method for forming carbon-carbon bonds. Its role in this reaction is crucial for creating new organic compounds and expanding the scope of chemical synthesis.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2-(Hydroxymethyl)-6-methoxyphenylboronic acid dehydrate is used as a key intermediate in the development of new drugs. Its unique reactivity allows for the creation of novel molecular structures with potential therapeutic applications.
Used in Material Science:
2-(Hydroxymethyl)-6-methoxyphenylboronic acid dehydrate is also utilized in the development of new materials. Its properties make it a valuable component in the synthesis of advanced materials with specific characteristics, such as improved mechanical strength or unique electronic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 947163-27-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,7,1,6 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 947163-27:
(8*9)+(7*4)+(6*7)+(5*1)+(4*6)+(3*3)+(2*2)+(1*7)=191
191 % 10 = 1
So 947163-27-1 is a valid CAS Registry Number.

947163-27-1SDS

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 1-hydroxy-7-methoxy-3H-2,1-benzoxaborole

1.2 Other means of identification

Product number -
Other names B-4920

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:947163-27-1 SDS

947163-27-1Upstream product

947163-27-1Downstream Products

947163-27-1Relevant articles and documents

ANDROGEN RECEPTOR MODULATOR COMPOUNDS AND METHODS

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Page/Page column 73; 121, (2008/06/13)

Provided herein are compounds that bind to androgen receptors and/or modulate activity of androgen receptors and/or modulate the amount of androgen receptors; and to methods for making and using such compounds. Also provided are compositions containing su

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