1721-59-1 (A’-新γ-马西群-22-醇,A'-Neogammaceran-22-ol)

快速询单

结构式：

A’-新γ-马西群-22-醇MOL文件

CAS号：

1721-59-1

中文名称：

A’-新γ-马西群-22-醇

英文名称：

A'-Neogammaceran-22-ol

分子式：

C₃₀H₅₂O

分子量：

428.733289718628

A’-新γ-马西群-22-醇(1721-59-1)名称与标识符

名称

英文别名：

A'-Neogammaceran-22-ol;17ß(H),21ß(H)-22-Hydroxyhopane;17ß(H),21ß(H)-22-Hydroxyhopaneneat;diplopterol;22-Hopanol;22-Hydroxyhopane;AC1L4VN4;AC1Q76LF;A'-neo-gammaceran-22-ol;Hopan-22-ol;hopane-22-ol;Hydroxyhopane;SureCN3201011;

标识符

InChIKey：

PNJBOAVCVAVRGR-UDCAXGDQSA-N

Inchi：

1S/C30H52O/c1-25(2)15-9-16-28(6)22(25)14-19-30(8)24(28)11-10-23-27(5)17-12-20(26(3,4)31)21(27)13-18-29(23,30)7/h20-24,31H,9-19H2,1-8H3/t20-,21-,22-,23+,24+,27-,28-,29+,30+/m0/s1

SMILES：

OC(C)(C)[C@H]1CC[C@@]2(C)[C@H]1CC[C@]1(C)[C@@H]2CC[C@@H]2[C@@]3(C)CCCC(C)(C)[C@@H]3CC[C@@]12C

A’-新γ-马西群-22-醇(1721-59-1)推荐厂家更多厂家(1)

公司名称	手机号/电话	联系人	QQ	微信	询单
深圳市中发源生物科技有限公司	18129803827 0755-23105005	林小姐	3158423203		询单

A’-新γ-马西群-22-醇(1721-59-1)相关文献

1. Lichens and fungi. Part II. Isolation and structural elucidation of 7β-acetoxy-22-hydroxyhopane from Sticta billardierii Del.
R. E. Corbett,H. Young J. Chem. Soc. C 1966 1556
2. Enzymatic synthesis of cyclic triterpenes
Ikuro Abe Nat. Prod. Rep. 2007 24 1311
3. Lichens and fungi. Part V. Dehydration rearrangements of 7-hydroxyhopanes
R. E. Corbett,R. A. J. Smith,H. Young J. Chem. Soc. C 1968 1823
4. Lichens and fungi. Part VI. Dehydration rearrangements of 15-hydroxyhopanes
R. E. Corbett,R. A. J. Smith J. Chem. Soc. C 1969 44
5. Lichens and Fungi. Part IV. Rearrangements at C-21 in the hopane series
R. E. Corbett,R. A. J. Smith J. Chem. Soc. C 1967 1622
6. Occurrence of triterpenoids in methanol-oxidizing bacteria. 2-Methyl-22 hydroxyhopane from Corynebacterium
André Babadjamian,Robert Faure,Michèle Laget,Gerard Dumenil,Prudent Padieu J. Chem. Soc. Chem. Commun. 1984 1657
7. Lichens and fungi. Part VII. Extractives from the lichen Sticta mougeotiana var. dissecta del
R. E. Corbett,Susan D. Cumming J. Chem. Soc. C 1971 955
8. Lichens and fungi. Part III. Structural elucidation of 15α,22-dihydroxyhopane from Sticta billardierii Del.
R. E. Corbett,H. Young J. Chem. Soc. C 1966 1564
9. 760. The chemistry of triterpenes and related compounds. Part XL. Final clarification of the stereochemistry of hydroxyhopanone
G. V. Baddeley,T. G. Halsall,E. R. H. Jones J. Chem. Soc. 1961 3891
10. Comparison of adipedatol with hydroxyhopane and hydroxyisohopane
H. Ageta,K. Shiojima Chem. Commun. (London) 1968 1372