6289-70-9 Usage
Uses
Used in Fragrance Industry:
(2E)-2-(phenylmethylidene)decanal is used as a fragrance ingredient for its pleasant odor, making it a popular component in perfumes, colognes, and other scented products.
Used in Pharmaceutical Industry:
(2E)-2-(phenylmethylidene)decanal is used as a potential pharmaceutical agent due to its potential applications in the development of new drugs and treatments.
Used in Cosmetic Industry:
(2E)-2-(phenylmethylidene)decanal is used as a component in cosmetic products for its pleasant scent and potential antimicrobial and antioxidant properties.
Used in Natural Product Chemistry and Biotechnology:
(2E)-2-(phenylmethylidene)decanal is used as a subject of interest in the field of natural product chemistry and biotechnology due to its potential antimicrobial and antioxidant properties, making it a candidate for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 6289-70-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6289-70:
(6*6)+(5*2)+(4*8)+(3*9)+(2*7)+(1*0)=119
119 % 10 = 9
So 6289-70-9 is a valid CAS Registry Number.
6289-70-9Relevant academic research and scientific papers
Direct β-C(sp3)-H Functionalization of Aliphatic Amines to α,β-Unsaturated Imines, Aldehydes, and Chromenes
Mandal, Sumana,Mahato, Sujit,Jana, Chandan K.
supporting information, p. 3762 - 3765 (2015/08/18)
A metal-free method for direct β-C(sp3)-H functionalization of aliphatic amine was developed. The method is based on a reaction that yields enamine directly from the corresponding aliphatic amine, which otherwise requires the aid of metallic reagent and/or external oxidant. The reaction is operationally simple, general, and highly efficient in functionalizing both cyclic and acyclic amines. Structurally diverse unsaturated imines were obtained from N-heterocycles, while acyclic amines provided 2-alkyl cinnamaldehyde and benzopyran derivatives with excellent E/Z-selectivity.
