trans-1-Decalone

Base Information

Chemical Name:trans-1-Decalone
CAS No.:936-18-5
Molecular Formula:C₁₀H₁₆O
Molecular Weight:152.236
Hs Code.:
European Community (EC) Number:244-352-5
UNII:22P3A7D875
DSSTox Substance ID:DTXSID301030742
Nikkaji Number:J353.702A

Synonyms:trans-1-Decalone;21370-71-8;trans-Bicyclo(4.4.0)decan-1-one;(4aR,8aS)-3,4,4a,5,6,7,8,8a-octahydro-2H-naphthalen-1-one;22P3A7D875;trans-Decahydro-1-naphthalenone;starbld0016699;trans-1-Decalone, 98%;SCHEMBL895510;UNII-22P3A7D875;(4aalpha,8abeta)-Decalin-1-one;DTXSID301030742;EINECS 244-352-5;AKOS024348816;J-014015;REL-(4AR,8AS)-OCTAHYDRO-1(2H)-NAPHTHALENONE;1(2H)-NAPHTHALENONE, OCTAHYDRO-, (4AR,8AS)-REL-

Suppliers and Price of trans-1-Decalone

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 0 raw suppliers

Chemical Property of trans-1-Decalone

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:152.120115130
Heavy Atom Count:11
Complexity:162

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC2C(C1)CCCC2=O
Isomeric SMILES:C1CC[C@H]2[C@H](C1)CCCC2=O

Technology Process of trans-1-Decalone

There total 3 articles about trans-1-Decalone 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:

: 936-17-4,936-18-5,3131-05-3,4832-16-0,5784-57-6,6102-29-0,6102-32-5,21370-71-8,32166-40-8
(4aS,8aΞ)-octahydro-naphthalen-1-one

Guidance literature:: (4) 1. Li, NH4Cl in fl. NH3, Birch-Red. 2. CrO3, Oxid.;
DOI:10.1139/v71-523

Reference yield:

: 21370-71-8
trans-1-decalone

: 6102-29-0
(9R,10S)-(+)-trans-1-decalone

: 52079-69-3,207127-50-2,691892-12-3
1c.9c.10t-α-Dekalol

: 936-18-5
trans-1-decalone

: 3275-81-8,207127-50-2,691892-12-3
(1S,4aS,8aR)-decahydronaphthalen-1-ol

Guidance literature:: With formate dehydrogenase from Candida boidinii; ammonium formate; Ca7β-hydroxysteroid dehydrogenase from Clostridium absonum; nicotinamide adenine dinucleotide phosphate; In aq. phosphate buffer; dimethyl sulfoxide; at 25 ℃; pH=7; enantioselective reaction; Enzymatic reaction;
DOI:10.1002/adsc.202000120

Reference yield:

: 21370-71-8
trans-1-decalone

: 6102-29-0
(9R,10S)-(+)-trans-1-decalone

: 52079-69-3,207127-50-2,691892-12-3
1c.9c.10t-α-Dekalol

: 936-18-5
trans-1-decalone

: 54422-07-0,207127-50-2,691892-12-3
(1R,4aS,8aR)-decahydronaphthalen-1-ol

Guidance literature:: With formate dehydrogenase from Candida boidinii; ammonium formate; Cae7β-hydroxysteroid dehydrogenase from Collinsella aerofaciens; nicotinamide adenine dinucleotide phosphate; In aq. phosphate buffer; dimethyl sulfoxide; at 25 ℃; pH=7; enantioselective reaction; Enzymatic reaction;
DOI:10.1002/adsc.202000120