(3beta,20beta)-3-acetoxy-11-oxoolean-12-en-29-oic acid

(3beta,20beta)-3-acetoxy-11-oxoolean-12-en-29-oic acid 구조식 이미지
카스 번호:
6277-14-1
상품명:
(3beta,20beta)-3-acetoxy-11-oxoolean-12-en-29-oic acid
동의어(영문):
Acetoxolone;Einecs 228-475-1;Acetylglycyrrhetic acid;Glycyrrhetic acid acetate;acetylglycyrrhetinic acid;29728-34-5 (Aluminum salt);3-Acetyl-18-beta-glycyrrhetinic acid;3-O-Acetyl-18beta-glycyrrhetinic acid;3β-(Acetyloxy)-11-oxoolean-12-en-30-oic acid;(20S)-3β-(Acetyloxy)-11-oxoolean-12-en-29-oic acid
CBNumber:
CB8928357
분자식:
C32H48O5
포뮬러 무게:
512.72
MOL 파일:
6277-14-1.mol

(3beta,20beta)-3-acetoxy-11-oxoolean-12-en-29-oic acid 속성

녹는점
322-325°
알파
D20 +141°
끓는 점
597.0±50.0 °C(Predicted)
밀도
1.14±0.1 g/cm3(Predicted)
증기압
0-0Pa at 20-30℃
산도 계수 (pKa)
4.71±0.70(Predicted)
LogP
4.77 at 35℃ and pH2.25

안전

(3beta,20beta)-3-acetoxy-11-oxoolean-12-en-29-oic acid C화학적 특성, 용도, 생산

Originator

Oriens ,Inverni Beffa ,Italy ,1981

Manufacturing Process

The salts of 3-acetyl-18β-glycyrrhetinic acid can be prepared by reaction between 3-acetyl-18β-glycyrrhetinic acid and an aluminum alcoholate. Preferably lower alcoholates are used, i.e., alcoholates in which the alkoxy group or groups have from one to four carbon atoms. The salification reaction may be carried out at room temperature or at an elevated temperature in conventional fashion, preferably in the presence of organic solvents. As organic solvents may be used alcohols, ethers, ketones, chlorinated solvents (methylene chloride, chloroform) ethyl acetate, etc.

Therapeutic Function

Antiulcer

(3beta,20beta)-3-acetoxy-11-oxoolean-12-en-29-oic acid 준비 용품 및 원자재

원자재

준비 용품


(3beta,20beta)-3-acetoxy-11-oxoolean-12-en-29-oic acid 공급 업체

글로벌( 3)공급 업체
공급자 전화 이메일 국가 제품 수 이점
Shanghai Zheyan Biotech Co., Ltd.
18017610038
zheyansh@163.com CHINA 3620 58
Shanghai Synchem Pharma Co., ltd 021-61984905-1 18016477331
synchempharma@aliyun.com China 6454 55
Wuhan Huangzhen Biochemical Co., Ltd 13795480948
3450865996@qq.com China 4958 58

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