Unisol

Base Information

Chemical Name:Unisol
CAS No.:36065-09-5
Molecular Formula:C17H20O
Molecular Weight:240.345
Hs Code.:
European Community (EC) Number:252-856-1,239-139-9
Nikkaji Number:J428.963C
Mol file:36065-09-5.mol

Synonyms:Unisol;EINECS 252-856-1;36065-09-5;Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-3-(phenylmethylene)-, (1R,4S)-;(+)-1,7,7-Trimethyl-3-(phenylmethylene)bicyclo(2.2.1)heptan-2-one;C17-H20-O;Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-3-(phenylmethylene)-, (1R,4S)-;(+)-1,7,7-Trimethyl-3-(phenylmethylene)bicyclo[2.2.1]heptan-2-one;Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-3-(phenylmethylene)-, (+)-;Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-3-(phenylmethylene)-, (+)-;Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-3-(phenylmethylene)-, (++)-;15087-24-8;(1R,4S)-3-Benzylidenebornan-2-one

Suppliers and Price of Unisol

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 4 raw suppliers

Chemical Property of Unisol

Chemical Property:

Vapor Pressure:3.34E-05mmHg at 25°C
Boiling Point:354.5°C at 760 mmHg
Flash Point:158.2°C
PSA：17.07000
Density:1.079g/cm³
LogP:4.09520
XLogP3:4.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:240.151415257
Heavy Atom Count:18
Complexity:398

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(C2CCC1(C(=O)C2=CC3=CC=CC=C3)C)C
Isomeric SMILES:C[C@@]12CC[C@@H](C1(C)C)/C(=C/C3=CC=CC=C3)/C2=O
Recent ClinicalTrials:A Phase 2, Open-Label, Randomized, Parallel Group, Placebo-Controlled, Single-Center Study to Assess Anti-microbial Efficacy and Safety of DCN01 Compared to Unisol? Following Topical Periocular Administration in Healthy Volunteers

Technology Process of Unisol

There total 15 articles about Unisol 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: 91.0%

: phenylmagnesium bromide

: 473929-46-3
(1R,4R)-3-[(E)-(dimethylamino)methylidene]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

: 15087-24-8,28070-26-0,31020-79-8,36065-09-5,36065-10-8,36275-29-3,79389-58-5,79389-62-1
(1R,4S,3E)-3-benzylidene-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

Guidance literature:: In tetrahydrofuran; at -78 - 20 ℃;
DOI:10.1016/j.tetasy.2006.04.014

Reference yield: 77.0%

: 100-52-7
benzaldehyde

: 74636-48-9
C₁₀H₁₄LiO^(1-)*Li⁽¹⁺⁾

: 28070-26-0,31020-79-8,36065-09-5,36065-10-8,36275-29-3,79389-58-5,79389-62-1,15087-24-8
trans-benzylidene-3-camphor

Guidance literature:: In diethyl ether; -78 deg C -> room temperature;
DOI:10.1021/ja00370a073

Reference yield: 71.0%

: 464-43-7
d-borneol

: 100-51-6,185532-71-2
benzyl alcohol

: 36065-09-5
1,7,7-trimethyl-3-(1-phenylmethylidene)bicyclo[2.2.1]heptan-2-one

Guidance literature:: With potassium hydroxide; dichlorotetrakis(dimethyl sulfoxide)ruthenium(II); In 1,4-dioxane; at 80 ℃; for 168h;
DOI:10.1016/j.tet.2006.07.012