(R)-Indenestrol A

Base Information

Chemical Name:(R)-Indenestrol A
CAS No.:115217-03-3
Molecular Formula:C₁₈H₁₈O₂
Molecular Weight:266.34
Hs Code.:
UNII:IIE442VRDN
DSSTox Substance ID:DTXSID501316334
Nikkaji Number:J398.542C
Wikidata:Q27115751
ChEMBL ID:CHEMBL306290
Mol file:115217-03-3.mol

Synonyms:(R)-Indenestrol A;115217-03-3;Ind AR;(+)-indenestrol A;Indenestrol A, (+)-;UNII-IIE442VRDN;IIE442VRDN;CHEBI:34012;1H-Inden-6-ol, 3-ethyl-2-(4-hydroxyphenyl)-1-methyl-, (R)-;(R)-3-Ethyl-2-(4-hydroxyphenyl)-1-methyl-1H-inden-6-ol;(+)-3-Ethyl-2-(4-hydroxyphenyl)-1-methyl-1H-inden-6-ol;BIDD:ER0015;(3R)-1-ethyl-2-(4-hydroxyphenyl)-3-methyl-3H-inden-5-ol;R-indenestrol A;CHEMBL306290;(R)-(+)-INDENESTROL A;DTXSID501316334;Q27115751;1H-Inden-6-ol, 3-ethyl-2-(4-hydroxyphenyl)-1-methyl-, (1R)-

Suppliers and Price of (R)-Indenestrol A

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 1 raw suppliers

Chemical Property of (R)-Indenestrol A

Chemical Property:

Vapor Pressure:2.46E-08mmHg at 25°C
Boiling Point:439.5°Cat760mmHg
Flash Point:207.6°C
PSA：40.46000
Density:1.176g/cm³
LogP:4.53570
XLogP3:3.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:266.130679813
Heavy Atom Count:20
Complexity:379

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1=C(C(C2=C1C=CC(=C2)O)C)C3=CC=C(C=C3)O
Isomeric SMILES:CCC1=C([C@@H](C2=C1C=CC(=C2)O)C)C3=CC=C(C=C3)O

Technology Process of (R)-Indenestrol A

There total 4 articles about (R)-Indenestrol A 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:

: 13029-44-2
dienestrol

: 115217-03-3,115217-02-2
[3H]-(+)-Indenestrol A

Guidance literature:: Multi-step reaction with 2 steps

1: 2 h / 240 °C

DOI:10.1248/cpb.40.588

Reference yield:

: 56-53-1,8053-00-7
diethylstilbestrol

: 115217-03-3,115217-02-2
[3H]-(+)-Indenestrol A

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent Spectr_. / DDQ / dioxane / 5 h / Heating

2: 2 h / 240 °C

With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In 1,4-dioxane;
DOI:10.1248/cpb.40.588