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76646-42-9

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76646-42-9 Usage

General Description

3-HYDROXYMETHYL-4-METHOXY-BENZALDEHYDE is a chemical compound with the molecular formula C9H10O3. It is a white to off-white crystalline substance with a melting point of 82-84°C. 3-HYDROXYMETHYL-4-METHOXY-BENZALDEHYDE is commonly used as a flavoring agent and fragrance in the food and cosmetic industries. It has a sweet, floral aroma with a hint of almond, making it a popular choice for adding aroma and flavor to various products. Additionally, it has been studied for its potential biological activities, including antimicrobial and antioxidant properties, which make it a versatile and valuable chemical in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 76646-42-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,4 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76646-42:
(7*7)+(6*6)+(5*6)+(4*4)+(3*6)+(2*4)+(1*2)=159
159 % 10 = 9
So 76646-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O3/c1-12-9-3-2-7(5-10)4-8(9)6-11/h2-5,11H,6H2,1H3

76646-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(hydroxymethyl)-4-methoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-Hydroxymethyl-4-methoxy-benzaldehyde

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:76646-42-9 SDS

76646-42-9Relevant articles and documents

Alkylation of NH-, OH-, and SH-acids in the presence of potassium carbonate: 1. Functionalization of chloromethyl group of alkoxy-substituted aromatic aldehydes

Khachatryan,Razinov,Kolotaev,Belus?,Matevosyan

, p. 395 - 404 (2015/10/29)

An easily scalable, economocal, and more safe method for the preparation of 3-chloromethyl-4-methoxybenzaldehyde was developed. The latter was subjected to reactions with NH-, OH-, and SH-acids in the presence of potassium carbonate to obtain new aromatic aldehydes in high yields.

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