Benzo(6,7)phenanthro(1,2-b)oxirene-10,11-diol, 1a,10,11,11a-tetrahydro-, (1aalpha,10beta,11alpha,11aalpha)-

Base Information

Chemical Name:Benzo(6,7)phenanthro(1,2-b)oxirene-10,11-diol, 1a,10,11,11a-tetrahydro-, (1aalpha,10beta,11alpha,11aalpha)-
CAS No.:76094-81-0
Molecular Formula:C18H14O3
Molecular Weight:278.302
Hs Code.:
DSSTox Substance ID:DTXSID10226976
Wikidata:Q83106568

Synonyms:76094-81-0;Benzo(6,7)phenanthro(1,2-b)oxirene-10,11-diol, 1a,10,11,11a-tetrahydro-, (1aalpha,10beta,11alpha,11aalpha)-;DTXSID10226976;1a,10,11,11a-Tetrahydrobenzo(6,7)phenanthro(1,2-b)oxirene-10,11-diol (1aalpha,10beta,11alpha,11aalpha)-

Suppliers and Price of Benzo(6,7)phenanthro(1,2-b)oxirene-10,11-diol, 1a,10,11,11a-tetrahydro-, (1aalpha,10beta,11alpha,11aalpha)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of Benzo(6,7)phenanthro(1,2-b)oxirene-10,11-diol, 1a,10,11,11a-tetrahydro-, (1aalpha,10beta,11alpha,11aalpha)-

Chemical Property:

Vapor Pressure:1.03E-13mmHg at 25°C
Boiling Point:567.5°Cat760mmHg
Flash Point:297°C
Density:1.478g/cm³
XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:278.094294304
Heavy Atom Count:21
Complexity:425

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C=C3C(=CC2=C1)C=CC4=C3C(C(C5C4O5)O)O
Isomeric SMILES:C1=CC=C2C=C3C(=CC2=C1)C=CC4=C3[C@H]([C@@H]([C@@H]5[C@H]4O5)O)O

Technology Process of Benzo(6,7)phenanthro(1,2-b)oxirene-10,11-diol, 1a,10,11,11a-tetrahydro-, (1aalpha,10beta,11alpha,11aalpha)-

There total 1 articles about Benzo(6,7)phenanthro(1,2-b)oxirene-10,11-diol, 1a,10,11,11a-tetrahydro-, (1aalpha,10beta,11alpha,11aalpha)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 64530-45-6,64838-75-1,64869-93-8,76094-80-9,76094-81-0
C₁₈H₁₄O₃

Guidance literature:: aus Alken 7 ueber Bromhydrin mit tert.-BuOK;
DOI:10.1016/S0040-4039(01)83773-4

Reference yield: 77.0%

: 76094-81-0
C₁₈H₁₄O₃

: 105880-23-7,78326-53-1,82050-47-3,86513-57-7,86513-59-9,86513-60-2,86513-61-3,86513-62-4,86513-63-5,86513-64-6,87099-89-6
r-1,t-2,3-c-4-tetrahydroxy-1,2,3,4-tetrahydrobenz anthracene

: 78326-53-1,82050-47-3,86513-57-7,86513-59-9,86513-60-2,86513-61-3,86513-62-4,86513-63-5,86513-64-6,87099-89-6
(1S,2R,3R,4R)-1,2,3,4-Tetrahydro-benzo[a]anthracene-1,2,3,4-tetraol

Guidance literature:: With water; oxonium; In 1,4-dioxane; at 25 ℃; Rate constant; Product distribution; hydrolysis, without catalysts;
DOI:10.1021/ja00313a044