195194-58-2 Usage
Description
(2S,3R)-2-N-acetylamino-1,3-dihydroxyoctadec-4-ene is a complex chemical compound derived from the fatty acid octadec-4-ene, featuring a 2S,3R stereochemistry and additional functional groups such as N-acetylamino and 1,3-dihydroxy. The unique structure and properties of this compound make it a promising candidate for various biological and pharmaceutical applications.
Uses
Used in Pharmaceutical Industry:
(2S,3R)-2-N-acetylamino-1,3-dihydroxyoctadec-4-ene is used as a pharmaceutical agent for its unique biochemical properties. The specific stereochemistry and functional groups of the compound may allow it to interact with biological systems in novel ways, potentially leading to the development of new drugs and therapies.
Used in Research and Development:
(2S,3R)-2-N-acetylamino-1,3-dihydroxyoctadec-4-ene is used as a research compound to study its interactions with biological systems and to explore its potential uses in various applications. Further research may be needed to fully understand its properties and to develop methods for its synthesis and application.
Check Digit Verification of cas no
The CAS Registry Mumber 195194-58-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,1,9 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 195194-58:
(8*1)+(7*9)+(6*5)+(5*1)+(4*9)+(3*4)+(2*5)+(1*8)=172
172 % 10 = 2
So 195194-58-2 is a valid CAS Registry Number.
195194-58-2Relevant articles and documents
Synthesis of two pairs of enantiomeric C18-sphingosines
Shibuya,Kawashima,Ikeda,Kitagawa
, p. 7205 - 7208 (2007/10/02)
Two pairs of enantiomeric (D-erythro, L-erythro, D-threo, L-threo) C18-sphingosines have been synthesized from Z-butene-1,4-diol utilizing Sharpless asymmetric epoxidation and a regiospecific ring-opening reaction of the resulting C4-chiral epoxide with an azide anion.
