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1036388-66-5

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1036388-66-5 Usage

Physical state

Colorless, crystalline solid

Derivation

From lignin, a complex organic polymer found in plant cell walls

Common uses

Production of pharmaceuticals, perfumes, and other fine chemicals

Industrial applications

Mediator in enzymatic reactions, substrate for determining lignin-degrading potential of microorganisms

Properties

Exhibits antioxidant and antimicrobial properties, making it valuable in various industrial and biological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1036388-66-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,3,8 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1036388-66:
(9*1)+(8*0)+(7*3)+(6*6)+(5*3)+(4*8)+(3*8)+(2*6)+(1*6)=155
155 % 10 = 5
So 1036388-66-5 is a valid CAS Registry Number.

1036388-66-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-Methoxy-4-methylphenyl)ethanol

1.2 Other means of identification

Product number -
Other names 2-(4-Hydroxy-3-methoxy-phenyl)-1H-benzoimidazole-4-carboxylic 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:1036388-66-5 SDS

1036388-66-5Downstream Products

1036388-66-5Relevant articles and documents

Synthesis of Functionalized Dihydrobenzofurans by Direct Aryl C?O Bond Formation under Mild Conditions

Alvarado, Joseph,Fournier, Jeremy,Zakarian, Armen

supporting information, p. 11625 - 11628 (2016/10/24)

A method for the synthesis of dihydrobenzofurans by a direct aryl C?O bond formation is described. A mechanistic pathway for the reaction, distinct from previously described similar transformations, allows for mild reaction conditions that are expected to be compatible with functionalized substrates.

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