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1,3-Benzenedicarboxaldehyde, 2-hydroxy-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5186-35-6

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5186-35-6 Usage

Appearance

White to pale yellow crystalline solid

Odor

Pleasant, sweet, and vanilla-like

Uses

a. Flavoring agent in food, beverages, and pharmaceuticals
b. Perfumes and cosmetics for its pleasant scent
c. Antimicrobial properties and used as a preservative

Synthesis

Derived from lignin, a natural polymer found in wood

Classification

Naturally occurring flavor compound

Check Digit Verification of cas no

The CAS Registry Mumber 5186-35-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5186-35:
(6*5)+(5*1)+(4*8)+(3*6)+(2*3)+(1*5)=96
96 % 10 = 6
So 5186-35-6 is a valid CAS Registry Number.

5186-35-6SDS

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 2-hydroxy-4-methylbenzene-1,3-dicarbaldehyde

1.2 Other means of identification

Product number -
Other names 1,3-Benzenedicarboxaldehyde,2-hydroxy-4-methyl

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:5186-35-6 SDS

5186-35-6Downstream Products

5186-35-6Relevant academic research and scientific papers

Biaryles dissymetriques par diformylation et aromatisation de cyclohexen-2-ones.

Labidalle, S.,Jean, E.,Moskowitz, H.,Miocque, M.,Thal,C.

, p. 2869 - 2870 (2007/10/02)

The classical procedure of formylation of ketones is reinvestigated in order to provide a synthetic route to unsymmetrical biaryls from cyclohexenones.

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