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2,3-DIMETHOXYCINNAMALDEHYDE, also known as 2,3-dimethoxycinnamaldehyde, is a yellow crystalline solid with a strong aromatic odor. It is a versatile chemical compound known for its sweet and spicy aroma, making it a popular choice as a flavoring agent in the food and beverage industry. Additionally, its unique scent has found applications in perfumery and fragrances. Moreover, scientific research has revealed its potential anti-inflammatory and anti-cancer properties, garnering interest in the pharmaceutical and medical fields. However, it is crucial to handle this substance with care due to its potential to irritate the eyes and skin upon contact.

62378-68-1

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62378-68-1 Usage

Uses

Used in Food and Beverage Industry:
2,3-DIMETHOXYCINNAMALDEHYDE is used as a flavoring agent for its sweet and spicy aroma, enhancing the taste and aroma of various food and beverage products.
Used in Perfumery and Fragrance Industry:
2,3-DIMETHOXYCINNAMALDEHYDE is used as a scent ingredient in perfumes and fragrances, contributing to the unique and appealing scents of these products.
Used in Pharmaceutical and Medical Research:
2,3-DIMETHOXYCINNAMALDEHYDE is used as a subject of scientific research for its potential anti-inflammatory and anti-cancer properties, with the aim of developing new treatments and therapies in the medical field.

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 academic research and scientific papers

Preparation method of 2, 3-dimethoxy cinnamaldehyde

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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.

Transition metal-catalyzed synthesis of pyrroles from dienyl azides

Dong, Huijun,Shen, Meihua,Redford, Joanne E.,Stokes, Benjamin J.,Pumphrey, Ashley L.,Driver, Tom G.

, p. 5191 - 5194 (2008/09/17)

(Chemical Equation Presented) A range of 2,5-disubstituted and 2,4,5-trisubstituted pyrroles can be synthesized from dienyl azides at room temperature using catalytic amounts of Znl2 or Rh2(O 2CC3F7)4.

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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