| Company Name: |
J & K SCIENTIFIC LTD.
|
| Tel: |
010-82848833 400-666-7788 |
| Email: |
jkinfo@jkchemical.com |
| Products Intro: |
Product Name:6'-Hydroxy Secophenol
CAS:2168-61-8
Package:10Mg,1Mg
|
| Company Name: |
Energy Chemical
|
| Tel: |
021-58432009 400-005-6266 |
| Email: |
marketing1@energy-chemical.com |
| Products Intro: |
Product Name:6'-Hydroxy Secophenol
CAS:2168-61-8
Purity:NULL Package:10mg;1mg Remarks:NULL
|
| Company Name: |
CLEARSYNTH LABS LTD.
|
| Tel: |
+91-22-45045900 |
| Email: |
sales@clearsynth.com |
| Products Intro: |
Product Name:6-Hydroxy Secophenol
CAS:2168-61-8
|
|
| | 6'-Hydroxy Secophenol Basic information |
| Product Name: | 6'-Hydroxy Secophenol | | Synonyms: | 6'-Hydroxy Secophenol;(3aS,4S,7aS)-4-[2-(2,3-dihydroxy-6-methylphenyl)ethyl]-7a-methyl-2,3,3a,4,6,7-hexahydroindene-1,5-dione;1H-Indene-1,5(4H)-dione, 4-[2-(2,3-dihydroxy-6-methylphenyl)ethyl]hexahydro-7a-methyl-, (3aS,4S,7aS)- | | CAS: | 2168-61-8 | | MF: | C19H24O4 | | MW: | 316.39 | | EINECS: | | | Product Categories: | Aromatics, Pharmaceuticals, Intermediates & Fine Chemicals | | Mol File: | 2168-61-8.mol |  |
| | 6'-Hydroxy Secophenol Chemical Properties |
| Boiling point | 512.8±50.0 °C(Predicted) | | density | 1.217±0.06 g/cm3(Predicted) | | pka | 10.07±0.40(Predicted) |
| | 6'-Hydroxy Secophenol Usage And Synthesis |
| Uses | 6''-Hydroxy Secophenol, is a derivative of Secophenol (S239550), that can be used for the synthesis of Cortistatins, which are the most potent congener, found to inhibit the proliferation of human umbilical vein endothelial cells with extreme selectivity among the cell lines. | | Uses | 6'-Hydroxy Secophenol, is a derivative of Secophenol (S239550), that can be used for the synthesis of Cortistatins, which are the most potent congener, found to inhibit the proliferation of human umbilical vein endothelial cells with extreme selectivity among the cell lines. | | Definition | ChEBI: 3,4-dihydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione is a seco-androstane that is 9,10-secoandrostane which is substituted by oxo groups at positions 9 and 17 and in which the A-ring is aromatic and bears hydroxy groups at positions 3 and 4. |
| | 6'-Hydroxy Secophenol Preparation Products And Raw materials |
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