2-Naphthalenecarboxylic acid, 1,2,3,4-tetrahydro-1-oxo-

Base Information

Chemical Name:2-Naphthalenecarboxylic acid, 1,2,3,4-tetrahydro-1-oxo-
CAS No.:62952-26-5
Molecular Formula:C11H10O3
Molecular Weight:190.199
Hs Code.:
DSSTox Substance ID:DTXSID90473087
Nikkaji Number:J938.208I

Synonyms:62952-26-5;2-Naphthalenecarboxylic acid, 1,2,3,4-tetrahydro-1-oxo-;SCHEMBL8021509;1-ketotetralin-2-carboxylic acid;DTXSID90473087;1-oxo-1,2,3,4-tetrahydro-2-naphthalenecarboxylic acid

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

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Chemical Property of 2-Naphthalenecarboxylic acid, 1,2,3,4-tetrahydro-1-oxo-

Chemical Property:

Boiling Point:393.3±31.0 °C(Predicted)
PSA：54.37000
Density:1.311±0.06 g/cm3(Predicted)
LogP:1.51630
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:190.062994177
Heavy Atom Count:14
Complexity:259

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC2=CC=CC=C2C(=O)C1C(=O)O

Technology Process of 2-Naphthalenecarboxylic acid, 1,2,3,4-tetrahydro-1-oxo-

There total 1 articles about 2-Naphthalenecarboxylic acid, 1,2,3,4-tetrahydro-1-oxo- 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: 3.0%

: 124-38-9,18923-20-1
carbon dioxide

: 123994-49-0
3,4-dihydro-1-naphthyl triflate

: 62952-26-5
1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid

: 529-34-0
3,4-dihydronaphthalene-1(2H)-one

: Carbonic acid mono-(3,4-dihydro-naphthalen-1-yl) ester

Guidance literature:: With nBuNBF₄; In N,N-dimethyl-formamide; at 20 ℃; electrochemical reaction;
DOI:10.1002/(sici)1099-0690(199809)1998:9<1811::aid-ejoc1811>3.0.co;2-v

Reference yield: 92.0%

: 91-01-0
1,1-Diphenylmethanol

: 62952-26-5
1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid

: 19399-43-0
2-benzhydryl-3,4-dihydronaphthalen-1(2H)-one

Guidance literature:: With iodine; In nitromethane; at 70 ℃; for 2h; Schlenk technique;
DOI:10.1039/c5ob01730k

Reference yield: 86.0%

: 2449-05-0
dibenzyl azodicarboxylate

: 62952-26-5
1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid

: dibenzyl (S)-1-(1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)hydrazine-1,2-dicarboxylate

Guidance literature:: With (9S,9"S)-9,9"-[phthalazine-1,4-diylbis-(oxy)]bis[10,11-dihydro-6'-methoxycinchonane]; In isopropyl alcohol; at 0 ℃; for 0.5h; enantioselective reaction; Schlenk technique;
DOI:10.1021/acs.orglett.7b00797