18472-36-1 Usage
Description
DELTA5-AVENASTEROL, also known as Δ5-Avenasterol, is a plant sterol analog of Stigmasterol (S686750). It is a naturally occurring compound found in various plants and is chemically similar to cholesterol. This similarity allows it to have potential applications in the pharmaceutical and chemical industries.
Uses
Used in Pharmaceutical Industry:
DELTA5-AVENASTEROL is used as a precursor in the synthesis of progesterone, a crucial hormone in the human body. It plays a significant role in the reproductive system, particularly during pregnancy, and is also used in the production of other steroidal medications.
DELTA5-AVENASTEROL is used as a starting material for [application type] in the pharmaceutical industry because of its structural similarity to cholesterol, which allows for the synthesis of important hormones and medications.
Used in Chemical Industry:
DELTA5-AVENASTEROL can also be used as an intermediate in the chemical industry for the production of various chemicals and compounds. Its unique structure makes it a valuable component in the synthesis of other complex molecules.
DELTA5-AVENASTEROL is used as an intermediate in the chemical industry for [application reason], such as the production of specific chemicals and compounds that require its unique structural properties.
Check Digit Verification of cas no
The CAS Registry Mumber 18472-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,7 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18472-36:
(7*1)+(6*8)+(5*4)+(4*7)+(3*2)+(2*3)+(1*6)=121
121 % 10 = 1
So 18472-36-1 is a valid CAS Registry Number.
InChI:InChI=1/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h7,10,19-20,23-27,30H,8-9,11-18H2,1-6H3
18472-36-1Relevant articles and documents
Stereochemical fate of C-26 and C-27 during the conversion of isofucosterol to sitosterol and of 24-methylenecholesterol to campesterol and dihydrobrassicasterol in Oryza sativa cell cultures
Nasu, Kozue,Takahashi, Kyoko,Morisaki, Masuo,Fujimoto, Yoshinori
, p. 381 - 385 (2007/10/03)
Administration of pro-R-methyl-13C-labeled isofucosterol to cultured cells of Oryza sativa revealed that the pro-R and pro-S methyls at C-25 become the pro-R and pro-S methyls at C-25 of sitosterol, respectively. Similar administration experime
Partial Synthesis of "Sargasterol" and (20S)-Cholesterol
Sucrow, Wolfgang,Nooy, Michael van
, p. 1897 - 1906 (2007/10/02)
The data of the synthetic (20S)-3β-hydroxy-5-cholestan-24-one (5b) and its acetate 5a differ significantly from those given for the degradation product of "sargasterol".The compounds 5a,b were converted into the E/Z-isomeric (20S)-stigmasta-5,24(28)-dien-3β-ols 8b, 9b, into their acetates 8a, 9a, and into (20S)-cholesterol (10b). (20S)-cholesterol acetate (10a) shows a lower melting point than that which is given in literature.
