Viscidulin C

Base Information

Chemical Name:Viscidulin C
CAS No.:35191-38-9
Molecular Formula:C15H20O4
Molecular Weight:264.3169
Hs Code.:
NSC Number:180027
DSSTox Substance ID:DTXSID20306814
Nikkaji Number:J19.175B
Wikidata:Q82054104
Mol file:35191-38-9.mol

Synonyms:NSC180027;35191-38-9;Viscidulin C;DTXSID20306814;NSC-180027

Suppliers and Price of Viscidulin C

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 3 raw suppliers

Chemical Property of Viscidulin C

Chemical Property:

Vapor Pressure:2.29E-09mmHg at 25°C
Boiling Point:434.3°C at 760 mmHg
Flash Point:163.8°C
PSA：59.06000
Density:1.27g/cm³
LogP:1.27850
XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:264.13615911
Heavy Atom Count:19
Complexity:473

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1C2C(CC(=C)C3CC4C(C3C2OC1=O)(O4)C)O

Technology Process of Viscidulin C

There total 4 articles about Viscidulin C 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:

: 82837-77-2
8-α-hydroxy-3(4),10(14)-dien 6,12-olide

: 35191-38-9
viscidulin C

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In chloroform; at 0 ℃; for 24h;
DOI:10.1016/0031-9422(82)80088-5

Reference yield:

: 81421-76-3
1αH,5αH,6βH,7αH,8α-hydroxyguai-4(15),10(14),11(13)-trien-6,12-olide

: 35191-38-9
viscidulin C

Guidance literature:: Multi-step reaction with 3 steps

1: 160 mg / Al amalgam / ethanol / 12 h / Heating

2: 110 mg / BF₃*Et₂O / benzene / 4 h / Ambient temperature

3: 45 mg / m-CPBA / CHCl₃ / 24 h / 0 °C

With aluminum amalgam; boron trifluoride diethyl etherate; 3-chloro-benzenecarboperoxoic acid; In ethanol; chloroform; benzene;
DOI:10.1016/0031-9422(82)80088-5

Reference yield:

: 81421-77-4
8α-hydroxyl-11βH-11,13-dihydrodehydrocostuslactone

: 35191-38-9
viscidulin C

Guidance literature:: Multi-step reaction with 2 steps

1: 110 mg / BF₃*Et₂O / benzene / 4 h / Ambient temperature

2: 45 mg / m-CPBA / CHCl₃ / 24 h / 0 °C

With boron trifluoride diethyl etherate; 3-chloro-benzenecarboperoxoic acid; In chloroform; benzene;
DOI:10.1016/0031-9422(82)80088-5