4651-48-3 (醋酸豆甾醇,Stigmasterol 3-Acetate)

快速询单

结构式：

醋酸豆甾醇MOL文件

CAS号：

4651-48-3

中文名称：

醋酸豆甾醇

英文名称：

Stigmasterol 3-Acetate

分子式：

C₃₁H₅₀O₂

分子量：

454.7275

醋酸豆甾醇(4651-48-3)名称与标识符

名称

中文别名：

醋酸豆甾醇;豆甾醇乙酸酯;

英文别名：

stigmasterol acetate;Stigmasterol 3-Acetate;3.β.-Acetoxystigmasta-5,22-diene;Stigmasterol 3-Aceta;Stigmasterylacetate;3β-Acetoxystigmasta-5,22-diene;-ol, acetate;stigmasta-5,22-dien-3-βStigmasta-5,22-dien-3β-yl acetate;

标识符

InChIKey：

IZEUIYYDWBKERE-ZRODXFKISA-N

Inchi：

InChI=1S/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/h9-11,20-21,23,25-29H,8,12-19H2,1-7H3/b10-9+/t21-,23-,25+,26+,27-,28+,29+,30+,31-/m1/s1

SMILES：

CC[C@H](/C=C/[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)OC(=O)C)C(C)C

醋酸豆甾醇(4651-48-3)物化性质

计算特性

氢键供体数量 : 0
氢键受体数量 : 2
可旋转化学键数量 : 7
重原子数量 : 33

醋酸豆甾醇(4651-48-3)推荐厂家更多厂家(15)

公司名称	手机号/电话	联系人	QQ	询单
湖北萃园生物科技有限公司	18162756256 027-84759766	金生 Jeremy	1197063825	询单
上海一基实业有限公司	13311756052 021-60526763 13311756052 13311756131	胡经理	2355265332	询单
上海一基实业有限公司	13311756131 021-60548336 QQ：2355265332 QQ:2851717387	胡经理	2355265332	询单
上海一基实业有限公司	13311756131 021-60548336 QQ：2355265332 QQ:2851717387	胡经理	2355265332	询单
赫澎（上海）生物科技有限公司	13122891558 186-16545970	张硕	3418426269	询单
上海甄准生物科技有限公司	13816009161 021-68920155	姜经理13816009161	3001086693	询单
金锦乐（湖南）化学有限公司		金锦乐	1226360695	询单
上海维亦特生物科技有限公司	15317051735	赵静	2033721411	询单
天成化工（江苏）有限公司	15251950002 0512-83500002	陈小姐		询单
四川维克奇生物科技有限公司	13348961525	杨洋	2851167780	询单

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1. GC-MS analysis of phytoconstituents from Ruellia prostrata and Senna tora and identification of potential anti-viral activity against SARS-CoV-2
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3. Biosynthesis of isoprenoids. Part III. Mechanism of alkylation during biosynthesis of stigmasterol in tissue cultures of higher plants
Yutaka Tomita,Atsuko Uomori J. Chem. Soc. Perkin Trans. 1 1973 2656
4. Mechanism of biosynthesis of the ethyl side-chain at C-24 of stigmasterol in tissue cultures of Nicotiana tabacum and Dioscorea tokoro
Yutaka Tomita,Atsuko Uomori J. Chem. Soc. D 1970 1416
5. Marine steroids. Part I. Structures of the principal aglycones from the saponins of the starfish, Marthasterias glacialis
Derek S. H. Smith,Alan B. Turner,Alexander M. Mackie J. Chem. Soc. Perkin Trans. 1 1973 1745
6. 380. The application of the method of molecular rotation differences to steroids. Part X. “β-Dihydroergosterol.”
D. H. R. Barton,J. D. Cox,N. J. Holness J. Chem. Soc. 1949 1771
7. A new method for the oxidation of alkenes to enones. An efficient synthesis of Δ5-7-oxo steroids
Anthony J. Pearson,Yong-Shing Chen,Gi Rin Han,Shih-Ying Hsu,Tapan Ray J. Chem. Soc. Perkin Trans. 1 1985 267
8. Ebenaceae extractives. Part IV. Diosindigo A, a blue pigment from several Diospyros species
Oliver C. Musgrave,Douglas Skoyles J. Chem. Soc. Perkin Trans. 1 1974 1128
9. 738. Triterpene resinols and related acids. Part XXVIII. The non-saponifiable fraction from Strychnos nux-vomica seed fat : the structure of cycloartenol
H. R. Bentley,J. A. Henry,D. S. Irvine,F. S. Spring J. Chem. Soc. 1953 3673
10. Biosynthesis of phytosterols in Calendula officinalis flowers from (2R)- and (2RS)-[2-14C, 2-3H]-mevalonic acid. The incorporation of a 15α-tritium atom into sitosterol
Jacek K. Sliwowski,Eliahu Caspi J. Chem. Soc. Chem. Commun. 1976 196