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

Base Information

Chemical Name:1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2R,5R)-rel-
CAS No.:130404-01-2
Deprecated CAS:66965-88-6
Molecular Formula:C₁₃H₂₂O
Molecular Weight:194.317
Hs Code.:
UNII:5U025YAZ3G,BH198C2TXE
DSSTox Substance ID:DTXSID90885888
Nikkaji Number:J415.515G
Wikidata:Q67880185

Synonyms:trans-Theaspirane;(2R,5R)-Theaspirane;Theaspirane, (2R,5R)-;BH198C2TXE;Theaspirane, trans-(+/-)-;5U025YAZ3G;(+/-)-Theaspirane, (E)-;43126-22-3;FEMA No. 3774, trans-(+/-)-;1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2R,5R)-;1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2R,5R)-rel-;1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2R-trans)-;130404-01-2;1-Oxaspiro[4.5]dec-6-ene, 2,6,10,10-tetramethyl-, (2R,5R)-rel-;UNII-5U025YAZ3G;UNII-BH198C2TXE;DTXSID90885888;Q67880185;trans-2,6,10,10-Tetramethyl-1-oxaspiro(4.5)dec-6-ene;1-OXASPIRO(4.5)DEC-6-ENE, 2,6,10,10-TETRAMETHYL-, TRANS-

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

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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

Chemical Property:

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:

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,5R)-rel-

There total 3 articles about 1-Oxaspiro(4.5)dec-6-ene, 2,6,10,10-tetramethyl-, (2R,5R)-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:

: 446293-94-3,3293-47-8
C₁₃H₂₄O

: 130404-01-2,43126-21-2,43126-22-3,66537-39-1,66537-40-4
theaspirane

: 43126-21-2,43126-22-3,66537-39-1,66537-40-4
theaspirane B

Guidance literature:: With selenium(IV) oxide; In 1,4-dioxane; at 60 ℃; for 1.5h;
DOI:10.1002/chem.201800315

Reference yield:

: 17283-81-7
4-(2,6,6-Trimethyl-cyclohex-1-enyl)-butan-2-on

: 130404-01-2,43126-21-2,43126-22-3,66537-39-1,66537-40-4
theaspirane

: 43126-21-2,43126-22-3,66537-39-1,66537-40-4
theaspirane B

Guidance literature:: Multi-step reaction with 3 steps

1: sodium tetrahydroborate

2: vinyl acetate

3: selenium(IV) oxide / 1,4-dioxane / 1.5 h / 60 °C

With selenium(IV) oxide; sodium tetrahydroborate; vinyl acetate; In 1,4-dioxane;
DOI:10.1002/chem.201800315

Reference yield:

: 446024-10-8
(R)-4-(2,6,6-trimethylcyclohex-1-enyl)butan-2-yl acetate

: 130404-01-2,43126-21-2,43126-22-3,66537-39-1,66537-40-4
theaspirane

: 43126-21-2,43126-22-3,66537-39-1,66537-40-4
theaspirane B

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / methanol; water

2: selenium(IV) oxide / 1,4-dioxane / 1.5 h / 60 °C

With selenium(IV) oxide; potassium hydroxide; In 1,4-dioxane; methanol; water;
DOI:10.1002/chem.201800315