1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2R,5S)-rel-

Base Information

Chemical Name:1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2R,5S)-rel-
CAS No.:43126-21-2
Deprecated CAS:66965-89-7
Molecular Formula:C13H22O
Molecular Weight:
Hs Code.:
UNII:9G9Q67D2IY,KW7I670C1V
Nikkaji Number:J415.514I
Wikidata:Q106940457
Mol file:43126-21-2.mol

Synonyms:(2S,5R)-Theaspirane;Theaspirane, (2S,5R)-;Theaspirane, cis-(+/-)-;KW7I670C1V;UNII-KW7I670C1V;9G9Q67D2IY;1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2R,5S)-rel-;43126-21-2;1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2S,5R)-;1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2S-cis)-;130404-02-3;cis-2,6,10,10-Tetramethyl-1-oxaspiro(4.5)dec-6-ene;UNII-9G9Q67D2IY;(+/-)-THEASPIRANE, CIS-;FEMA NO. 3774, CIS-(+/-)-;1-OXASPIRO(4.5)DEC-6-ENE, 2,6,10,10-TETRAMETHYL-, CIS-

Suppliers and Price of 1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2R,5S)-rel-

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
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price

Total 2 raw suppliers

Chemical Property of 1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2R,5S)-rel-

Chemical Property:

Vapor Pressure:0.0281mmHg at 25°C
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:194.167065321
Heavy Atom Count:14
Complexity:264

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1CCC2(O1)C(=CCCC2(C)C)C
Isomeric SMILES:C[C@H]1CC[C@]2(O1)C(=CCCC2(C)C)C

Technology Process of 1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2R,5S)-rel-

There total 50 articles about 1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2R,5S)-rel- 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: 95.0%

: 113110-02-4
3-(3-hydroxy-butyl)-2,4,4-trimethyl-cyclohex-2-enol

: 36431-72-8,59872-09-2,79516-57-7,169102-88-9,43126-21-2,43126-22-3,66537-39-1,66537-40-4
2,6,10,10-tetramethyl-1-oxaspiro[4.5]dec-6-ene

Guidance literature:: amberlyst-15; In chloroform; at -20 ℃;
DOI:10.1016/S0040-4039(00)00396-8

Reference yield: 70.0%

: 13720-37-1
dihydro-α-ionol

: 36431-72-8,59872-09-2,79516-57-7,169102-88-9,43126-21-2,43126-22-3,66537-39-1,66537-40-4
2,6,10,10-tetramethyl-1-oxaspiro[4.5]dec-6-ene

: 41678-32-4,63335-66-0,72746-44-2,74006-61-4,74006-62-5,122797-82-4
dl-dihydroedulan

Guidance literature:: With bis(p-chlorophenyl) diselenide; tetraethylammonium perchlorate; In water; acetonitrile; at 65 - 70 ℃; electrochemical oxidation;
DOI:10.1016/S0040-4039(00)98772-0

Reference yield: 24.0%

: 13720-37-1
dihydro-α-ionol

: 36431-72-8,59872-09-2,79516-57-7,169102-88-9,43126-21-2,43126-22-3,66537-39-1,66537-40-4
2,6,10,10-tetramethyl-1-oxaspiro[4.5]dec-6-ene

Guidance literature:: With Phenylselenyl chloride; tetraethylammonium perchlorate; In dichloromethane; electrochemical oxidation;
DOI:10.1016/S0040-4039(00)98772-0