83071-67-4 Usage
Description
4-Acetoxy-3-methoxycinnamaldehyde is a cinnamaldehyde derivative, which is an organic building block useful in chemical synthesis. It is characterized by the presence of an acetoxy group at the 4-position and a methoxy group at the 3-position, attached to a cinnamaldehyde backbone.
Uses
Used in Chemical Synthesis Industry:
4-Acetoxy-3-methoxycinnamaldehyde is used as a synthetic intermediate for the production of various organic compounds and pharmaceuticals. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of complex molecules.
Used in Flavor and Fragrance Industry:
Due to its aromatic properties, 4-Acetoxy-3-methoxycinnamaldehyde is used as a flavoring agent and a fragrance ingredient in the food, beverage, and cosmetics industries. Its distinct scent and taste profile contribute to the creation of unique and appealing products.
Used in Pharmaceutical Industry:
4-Acetoxy-3-methoxycinnamaldehyde is utilized as a key component in the development of pharmaceutical drugs. Its chemical properties enable it to be incorporated into drug molecules, potentially leading to the discovery of new therapeutic agents with novel mechanisms of action.
Used in Research and Development:
In the field of scientific research, 4-Acetoxy-3-methoxycinnamaldehyde serves as a valuable compound for studying various chemical reactions and processes. Its reactivity and structural features make it an ideal candidate for exploring new synthetic pathways and understanding reaction mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 83071-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,7 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83071-67:
(7*8)+(6*3)+(5*0)+(4*7)+(3*1)+(2*6)+(1*7)=124
124 % 10 = 4
So 83071-67-4 is a valid CAS Registry Number.
83071-67-4Relevant articles and documents
DDQ-mediated oxidation of allylarenes: Expedient access to cinnamaldehyde-containing phenylpropanoids
Jiang, Tao-Shan,Zhang, Qingqing,Li, Guohui,Cheng, Xi,Cai, Yongping
, p. 4611 - 4616 (2019/02/01)
Phenylpropanoid natural products containing a cinnamaldehyde motif were easily synthesized from allylarenes mediated by 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) oxidation. Representative examples described herein are five types of 4-hydroxycinnamaldehyde derivatives from monolignols biosynthesis, Boropinal C, and 7-methoxywutaifuranal from plant extracts. Especially, simple synthesis of 7-methoxywutaifuranal was exploited through selective mono-oxidation and subsequent isomerization-ring-closing-metathesis strategy.
Efficient preparation of trans-α,β-unsaturated aldehydes from saturated aldehydes by oxidative enamine catalysis
Zhang, Shilei,Xie, Hexin,Song, Aiguo,Wu, Deyan,Zhu, Jin,Zhao, Sihan,Li, Jian,Yu, Xinhong,Wang, Wei
experimental part, p. 1932 - 1936 (2012/03/09)
A mild and highly efficient amine-catalyzed, IBX-mediated oxidation of aldehydes to (E) selective α,β-unsaturated aldehydes has been achieved in good yields. The process features a new oxidation of enamines to iminium ions in a catalytic fashion.
Phase transfer Wittig reaction with 1,3-dioxolan-2-yl-methyltriphenyl phosphonium salts: An efficient method for vinylogation of aromatic aldehydes
Daubresse, Nicolas,Francesch, Charlette,Rolando, Christian
, p. 10761 - 10770 (2007/10/03)
Aldehydes were efficiently transformed into allylic dioxolanes by a Wittig-type reaction, using 1,3-dioxolan-2-yl-methyltriphenylphosphonium bromide under phase transfer conditions. The substituent kinetic effects were studied, and related to Hammett values and electrochemical potentials.
