922527-72-8 Usage
General Description
1,2-Undecanediol, 1-(4-methylbenzenesulfonate), (2R)- is a chemical compound that consists of a 1,2-undecanediol molecule with a 4-methylbenzenesulfonate group attached to it. The 1,2-undecanediol, also known as glycerol monoundecyl ether, is a long-chain diol commonly used in various industrial applications such as in the production of lubricants, plasticizers, and cosmetics. The 4-methylbenzenesulfonate group is a sulfonic acid derivative, and the (2R)- designation specifies the stereochemistry of the compound, indicating that it has a specific spatial arrangement of its atoms. 1,2-Undecanediol, 1-(4-methylbenzenesulfonate), (2R)- may have potential applications in the fields of organic synthesis, materials science, and pharmaceutical research due to its distinct chemical structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 922527-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,2,5,2 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 922527-72:
(8*9)+(7*2)+(6*2)+(5*5)+(4*2)+(3*7)+(2*7)+(1*2)=168
168 % 10 = 8
So 922527-72-8 is a valid CAS Registry Number.
922527-72-8Relevant academic research and scientific papers
Total synthesis of caminoside B, a novel antimicrobial glycolipid isolated from the marine sponge Caminus sphaeroconia
Zhang, Zaihong,Zong, Chengli,Song, Gaopeng,Lv, Guokai,Chun, Yuexing,Wang, Peng,Ding, Ning,Li, Yingxia
experimental part, p. 750 - 760 (2010/06/21)
The first total synthesis of caminoside B, a novel marine antimicrobial glycolipid isolated from the marine sponge Caminus sphaeroconia, was developed. This marine small molecule inhibitor (IC50 = 20 μM) targeting type III secretory pathway of
Studies towards lipid A: a synthetic strategy for the enantioselective preparation of 3-hydroxy fatty acids
Guaragna, Annalisa,Nisco, Mauro De,Pedatella, Silvana,Palumbo, Giovanni
, p. 2839 - 2841 (2007/10/03)
A short and efficient enantioselective synthesis of (R)-3-hydroxydodecanoic acid is described, involving a Sharpless asymmetric dihydroxylation to produce the required (R)-stereochemistry.
