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201471-76-3

1,2-Benzenediol, 3-bromo-6-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 201471-76-3 Structure

  • Basic information

    1. Product Name: 1,2-Benzenediol, 3-bromo-6-methyl- (9CI)
    2. Synonyms: 1,2-Benzenediol, 3-bromo-6-methyl- (9CI)
    3. CAS NO:201471-76-3
    4. Molecular Formula: C7H7BrO2
    5. Molecular Weight: 203.03328
    6. EINECS: N/A
    7. Product Categories: ALCOHOL
    8. Mol File: 201471-76-3.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,2-Benzenediol, 3-bromo-6-methyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Benzenediol, 3-bromo-6-methyl- (9CI)(201471-76-3)
    11. EPA Substance Registry System: 1,2-Benzenediol, 3-bromo-6-methyl- (9CI)(201471-76-3)

  • 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: 201471-76-3(Hazardous Substances Data)

201471-76-3 Usage

Type

Chemical compound

Derivative of

Catechol (a dihydroxy benzene)

Structure

Brominated and methylated form of catechol

Usage

Biochemical reagent in research and laboratory experiments

Properties

Exhibits antioxidant properties

Potential applications

Therapeutic applications in treating various diseases

Safety

Handled and stored following standard safety protocols due to potential hazards and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 201471-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,4,7 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 201471-76:
(8*2)+(7*0)+(6*1)+(5*4)+(4*7)+(3*1)+(2*7)+(1*6)=93
93 % 10 = 3
So 201471-76-3 is a valid CAS Registry Number.

201471-76-3SDS

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 3‐bromo‐6--methylbenzene‐1,2-‐diol

1.2 Other means of identification

Product number -
Other names 3-Bromo-6-methyl-benzene-1,2-diol

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:201471-76-3 SDS

201471-76-3Downstream Products

201471-76-3Relevant articles and documents

An enantioselective total synthesis of helioporins C and e

L?lsberg, Wibke,Werle, Susen,Neud?rfl, J?rg-Martin,Schmalz, Hans-Günther

, p. 5996 - 5999 (2013/02/23)

A short and enantioselective total synthesis of helioporins C and E, which are bioactive marine diterpenes containing a serrulatane or amphilectane skeleton, was elaborated. The chirogenic step, i.e. a Cu(I)-catalyzed allylic alkylation of a cinnamyl chlo

A convenient procedure for the synthesis of 1-tetralone dertivatives using a Suzuki coupling-Friedel-Crafts acylation sequence

Esteban, Gemma,Lopez-Sanchez, Miguel A.,Martinez, Ma. Eugenia,Plumet, Joaquin

, p. 197 - 212 (2007/10/03)

The reported 1-tetralone derivatives have been synthesized from arylbromides using as keys steps a Suzuki coupling followed by intramolecular Friedel-Crafts acylation.

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