117356-20-4 Usage
Description
(1R,2S,5R)-2-isopropyl-5-methylcyclohex-1-yl hydroxyacetate is a cyclohexane derivative featuring a cyclohexane ring with an isopropyl and a methyl group, along with an acetate group connected to a hydroxyl group. This colorless liquid with a pleasant odor is widely recognized in the fragrance and flavor industry.
Uses
Used in Fragrance and Flavor Industry:
(1R,2S,5R)-2-isopropyl-5-methylcyclohex-1-yl hydroxyacetate serves as a key ingredient in the fragrance and flavor industry, leveraging its pleasant odor to enhance the sensory experience of various products.
Used as a Precursor in Pharmaceutical and Agrochemical Synthesis:
In the synthesis of pharmaceuticals and agrochemicals, (1R,2S,5R)-2-isopropyl-5-methylcyclohex-1-yl hydroxyacetate acts as a valuable precursor, contributing to the development of new and improved products within these fields.
Used in Medical and Industrial Research:
Due to its unique molecular structure, (1R,2S,5R)-2-isopropyl-5-methylcyclohex-1-yl hydroxyacetate is extensively studied for potential applications in medicine and industry, with a focus on uncovering its specific biological activities and uses.
Check Digit Verification of cas no
The CAS Registry Mumber 117356-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,3,5 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 117356-20:
(8*1)+(7*1)+(6*7)+(5*3)+(4*5)+(3*6)+(2*2)+(1*0)=114
114 % 10 = 4
So 117356-20-4 is a valid CAS Registry Number.
117356-20-4Relevant articles and documents
Domino processes as a tool for recovering substandard reactions. Synthesis and use of nitroacetic acid esters and amides
Scardovi, Noemi,Casalini, Andrea,Peri, Francesca,Righi, Paolo
, p. 965 - 968 (2002)
(equation presented) Elusive nitroacetic acid esters and amides were obtained through a halogen exchange reaction of the corresponding bromoacetic acid derivatives with polymer-supported nitrite anion. The process is flawed by a side product catalyzed deg
