61229-06-9 Usage
Description
(5E)-7-methyloct-5-enoic acid is a carboxylic acid with a unique molecular structure, characterized as an unsaturated fatty acid with a chain of eight carbon atoms and a double bond at the fifth position. It is commonly found in natural sources such as plants and animals and is utilized in the production of various products, including food additives, pharmaceuticals, and fragrances.
Uses
Used in Food Additives Industry:
(5E)-7-methyloct-5-enoic acid is used as a flavoring agent for enhancing the taste and aroma of food products, capitalizing on its natural presence in certain plants and its ability to contribute to the overall sensory experience.
Used in Pharmaceutical Industry:
(5E)-7-methyloct-5-enoic acid is used as an active pharmaceutical ingredient for its potential health benefits and therapeutic applications, leveraging its unique structure and characteristics to address specific medical needs.
Used in Fragrance Industry:
(5E)-7-methyloct-5-enoic acid is used as a component in creating various fragrances, taking advantage of its natural occurrence in plants and its ability to contribute to the development of distinct and appealing scents.
Used in Industrial Applications:
(5E)-7-methyloct-5-enoic acid is used in various industrial processes due to its chemical properties, which make it a valuable component in the development and production of different products.
Check Digit Verification of cas no
The CAS Registry Mumber 61229-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,2 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61229-06:
(7*6)+(6*1)+(5*2)+(4*2)+(3*9)+(2*0)+(1*6)=99
99 % 10 = 9
So 61229-06-9 is a valid CAS Registry Number.
61229-06-9Relevant articles and documents
Total synthesis of (+)-epopromycin B and its analogues - Studies on the inhibition of cellulose biosynthesis
Dobler, Markus R.
, p. 215 - 218 (2007/10/03)
The described inhibition of the cellulose biosynthesis by epopromycin B prompted us to establish a short and efficient synthesis of the natural product, suitable for accessing a broad range of unnatural analogues in a multiparallel fashion. During the course of our synthesis the absolute configuration of (+)-epopromycin B could be determined.
An Alternate Synthesis of the Capsaicinoids
Kaga, Harumi,Goto, Kouhei,Fukuda, Takashi,Orito, Kazuhiko
, p. 946 - 948 (2007/10/02)
Five capsaicinoids, the pungent ingredients of hot peppers, have been efficiently synthesized by a method involving the Wittig reaction between isobutyl triphenylphosphorane and the appropriate lactols (3), followed by the nitrous acid-induced isomerization of the resultant (Z)-olefins (4) to (E)-olefins (5).
TRANS STEREOSELECTIVITY IN THE REACTION OF (4-CARBOXYBUTYLIDENE)TRIPHENYLPHOSPHORANE WITH AROMATIC ALDEHYDES
Maryanoff, Bruce E.,Duhl-Emswiler, Barbara A.
, p. 4185 - 4188 (2007/10/02)
Aromatic aldehydes react with 1 to give predominantly trans 6-aryl-5-hexenoic acids, under special conditions.A systematic study of the reaction of 1 with aldehydes, in a preliminary attempt to define the cause and scope of the trans stereoselectivity, is reported.
