4651-46-1 Usage
Uses
Used in Pharmaceutical Industry:
Alpha-Spinasterol acetate is used as a therapeutic agent for its anti-inflammatory, anti-microbial, and anti-oxidant properties, which contribute to the treatment of various diseases, including cancer and cardiovascular conditions.
Used in Nutraceutical Industry:
Alpha-Spinasterol acetate is used as a dietary supplement for its health-promoting properties, such as reducing inflammation and supporting cardiovascular health.
Used in Cosmetic Industry:
Alpha-Spinasterol acetate is used as an ingredient in skincare products for its anti-oxidant and anti-inflammatory properties, which can help protect the skin from environmental damage and promote a healthy complexion.
Used in Agricultural Industry:
Alpha-Spinasterol acetate is used as a natural pesticide or fungicide due to its anti-microbial properties, helping to protect crops from diseases and pests.
Used in Food Industry:
Alpha-Spinasterol acetate is used as a natural preservative in food products to extend shelf life and maintain freshness, as well as for its potential health benefits when consumed.
Check Digit Verification of cas no
The CAS Registry Mumber 4651-46-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,5 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4651-46:
(6*4)+(5*6)+(4*5)+(3*1)+(2*4)+(1*6)=91
91 % 10 = 1
So 4651-46-1 is a valid CAS Registry Number.
InChI:InChI=1/C31H50O2/c1-8-23(20(2)3)10-9-21(4)27-13-14-28-26-12-11-24-19-25(33-22(5)32)15-17-30(24,6)29(26)16-18-31(27,28)7/h9-10,12,20-21,23-25,27-29H,8,11,13-19H2,1-7H3/b10-9+/t21-,23-,24+,25+,27-,28+,29+,30+,31-/m1/s1
4651-46-1Relevant academic research and scientific papers
Rauwald, Hans-Willi,Sauter, Michael,Schilcher, Heinz
, p. 2746 - 2748 (1985)
In the seeds of Cucurbita pepo three closely related 24-ethyl-Δ7-steryl glucosides were identified by hydrolytic studies and spectral analysis as spinasteryl-β-D-glucopyranoside, the new 3-O-(β-D-glucopyranosyl)-24β-ethyl-5α-cholesta-7,25(27)-dien-3β-ol and the corresponding Δ22E,25(27)-trienol.Except for its occurence in cucumber seeds the latter is so far unknown as a natural product. Key Word Index - Cucurbita pepo; Cucurbitaceae; pumpkin; seeds; steryl glucosides; 3-O-(β-D-glucopyranosyl)-24β-ethyl-5α-cholesta-7,25(27)dien-3-β-ol; 3-O-(β-D-glucopyranosyl) -24β-ethyl-5α-cholesta-7,trans-22,25(27)-trien-3β-ol; spinasteryl-β-D-glucopyranoside.
Synthesis of Chondrillasterol and Spinasterol
Anastasia, Mario,Fiecchi, Alberto,Scala, Antonio,Puppo, Marina del
, p. 2561 - 2562 (2007/10/02)
Spinasterol (1a) and chondrillasterol (1b) have been synthesized from the ethyl (22E,24S)-and (22E,24R)-3β-acetoxy-5α-stigmasta-7,22-dien-29-oates, (2c) and (2d), respectively.
Constituents of Albizzia zygia
Schoppa, Thomas,Pachaly, Peter
, p. 18 - 25 (2007/10/02)
Lupen-20(30)-3β-ol (1), 14α-stigmast-5-en-3β-ol (3) and 5α-stigmast-7,22-dien-3β-ol (5) were isolated from the bark of Albizzia zygia (Mimosaceae).Leaves also contain these substances and, in addition, a glycoside of 1 as well as four further compounds which give a positive reaction with SbCl3.