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62378-68-1

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62378-68-1 Usage

General Description

2,3-DIMETHOXYCINNAMALDEHYDE, also known as 2,3-dimethoxycinnamaldehyde, is a yellow crystalline solid with a strong aromatic odor. It is commonly used as a flavoring agent in the food and beverage industry due to its sweet and spicy aroma. This chemical is also utilized in perfumery and fragrance applications for its unique scent. Additionally, 2,3-DIMETHOXYCINNAMALDEHYDE has shown potential anti-inflammatory and anti-cancer properties in scientific research, making it a subject of interest in the pharmaceutical and medical fields. However, it is essential to handle this substance with caution, as it can irritate the eyes and skin upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 62378-68-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,7 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62378-68:
(7*6)+(6*2)+(5*3)+(4*7)+(3*8)+(2*6)+(1*8)=141
141 % 10 = 1
So 62378-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O3/c1-13-10-7-3-5-9(6-4-8-12)11(10)14-2/h3-8H,1-2H3/b6-4+

62378-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Dimethoxycinnamaldehyde

1.2 Other means of identification

Product number -
Other names 2,3-Dimethoxy-trans-zimtaldehyd

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:62378-68-1 SDS

62378-68-1Downstream Products

62378-68-1Relevant articles and documents

Preparation method of 2, 3-dimethoxy cinnamaldehyde

-

Paragraph 0007-0010, (2019/01/24)

The invention relates to a preparation method of 2, 3-dimethoxy cinnamaldehyde, and belongs to the technical field of medicine, aiming at solving the technical problem of providing a relatively advanced preparation method of 2, 3-dimethoxy cinnamaldehyde.

Formation of acetaldehyde enolate from vinyl acetate and its reaction with aromatic and heterocyclic aldehydes: An efficient synthesis of enals and polyenals

Mahata,Barun,Ila,Junjappa

, p. 1345 - 1347 (2007/10/03)

Two carbon homologation of aromatic and heterocyclic aldehydes is achieved by reacting them with acetaldehyde enolate anion generated in situ by cleaving vinyl acetate in the presence of barium hydroxide.

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