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2 6-DIETHOXYTOLUENE 97 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6972-63-0

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6972-63-0 Usage

Physical state

Colorless liquid

Odor

Fruity

Common uses

Solvent in industrial processes

Applications

Paint and coating formulations, production of polymers and plastics, manufacturing of adhesives, sealants, and inks

Additional uses

Personal care products and pharmaceutical formulations

Characteristics

Ability to dissolve a wide range of substances

Check Digit Verification of cas no

The CAS Registry Mumber 6972-63-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6972-63:
(6*6)+(5*9)+(4*7)+(3*2)+(2*6)+(1*3)=130
130 % 10 = 0
So 6972-63-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O2/c1-4-12-10-7-6-8-11(9(10)3)13-5-2/h6-8H,4-5H2,1-3H3

6972-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-diethoxy-2-methylbenzene

1.2 Other means of identification

Product number -
Other names 2,6-Diaethoxy-toluol

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:6972-63-0 SDS

6972-63-0Relevant academic research and scientific papers

Synthesis of cribrostatin 6

Markey, Michael D.,Kelly, T. Ross

supporting information; experimental part, p. 7441 - 7443 (2009/04/11)

(Chemical Equation Presented) The synthesis of cribrostatin 6 (1) is described. A regioselective bromination, a biaryl coupling, and an intramolecular cyclization are the key steps in the synthesis.

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