90646-67-6 Usage
Uses
Used in Pharmaceutical Industry:
(2Z)-3-methyloct-2-enoic acid is used as a bioactive compound for its potential therapeutic effects. Its hydrophobic nature and ability to penetrate bio-membranes make it a promising candidate for drug delivery and development.
Used in Cosmetics Industry:
(2Z)-3-methyloct-2-enoic acid is used as an ingredient in cosmetic formulations for its potential benefits to the skin. Its hydrophobic properties may contribute to improved skin penetration and enhanced effectiveness of cosmetic products.
Used in Other Industries:
(2Z)-3-methyloct-2-enoic acid may also find applications in other industries where its unique properties can be utilized, such as in the development of new materials or in chemical processes that require hydrophobic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 90646-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,4 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90646-67:
(7*9)+(6*0)+(5*6)+(4*4)+(3*6)+(2*6)+(1*7)=146
146 % 10 = 6
So 90646-67-6 is a valid CAS Registry Number.
90646-67-6Relevant academic research and scientific papers
4-endo-trig cyclization processes using bis(collidine)bromine(i) hexafluorophosphate as reagent: Preparation of 2-oxetanones, 2-azetidinones, and oxetanes
Homsi, Fadi,Rousseau, Gerard
, p. 81 - 85 (2007/10/03)
Reaction in methylene chloride of bis(collidine)bromine(I) hexafluorophosphate with α,β-unsaturated acids and α,β-unsaturated N- sulfonamides was found to lead diastereospecifically to the corresponding 2- oxetanones and 2-azetidinones in moderate yields (23-60%), by an almost unknown 4-endo cyclization. This process allow the synthesis of these interesting classes of products in one step from common substrates. Similarly, the reaction of cinnamic alcohols led, by the same cyclization procedure, to oxetanes (20-36%); the presence of a gem-dimethyl group in α of the alcohol function appeared beneficial.
