127604-16-4 Usage
Description
(S)-3-HYDROXYBUTYRIC ACID SODIUM SALT, also known as Sodium (S)-3-Hydroxybutyrate, is an organic sodium salt compound derived from (S)-3-hydroxybutyric acid. It is a chiral molecule with a specific stereochemistry, which is crucial for its applications and properties.
Used in Pharmaceutical Industry:
(S)-3-HYDROXYBUTYRIC ACID SODIUM SALT is used as a chemical intermediate for the preparation of dideoxymycobactin (DDM), a compound with potential applications in the development of new drugs and therapies.
Used in Chemical Synthesis:
(S)-3-HYDROXYBUTYRIC ACID SODIUM SALT is used as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and reactivity make it a valuable component in the creation of complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 127604-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,6,0 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127604-16:
(8*1)+(7*2)+(6*7)+(5*6)+(4*0)+(3*4)+(2*1)+(1*6)=114
114 % 10 = 4
So 127604-16-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H8O3.Na/c1-3(5)2-4(6)7;/h3,5H,2H2,1H3,(H,6,7);/q;+1/p-1/t3-;/m0./s1
127604-16-4Relevant articles and documents
Preparation of Stereochemically Pure Sex Pheromone Components of the Pine Sawfly (Neodiprion sertifer) and Field Tests of the Synthetic Compounds
Tai, Akira,Morimoto, Naotake,Yoshikawa, Masato,Uehara, Kazuya,Sugimura, Takashi,Kikukawa, Tadashi
, p. 1753 - 1762 (2007/10/02)
Stereochemically pure pheromone components of the pine sawfly, acetates of (2S,3S,7S)- and (2S,3R,7R)-3,7-dimethylpentadecan-2-ol, were prepared by an improved synthetic procedure.Mixtures of the newly prepared compounds were tested in the field (red pine forests in Hyogo and Nagano, Japan) for their attraction of Neodiprion sertifer.The maximum response was observed in mixtures of the ratio (2S,3R,7R)/(2S,3S,7S)-10-3: 1 to 10-4: 1.When the results are compared with those in Michigan, U.S.A., N. sertifer in Japan responded less specifically to certain blending ratios of diastereomers than in America.
