550515
3-Oxo-1-cyclohexanecarboxylic acid
93%
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About This Item
Linear Formula:
C6H9(O)CO2H
CAS Number:
Molecular Weight:
142.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
3-Oxo-1-cyclohexanecarboxylic acid, 93%
InChI
1S/C7H10O3/c8-6-3-1-2-5(4-6)7(9)10/h5H,1-4H2,(H,9,10)
SMILES string
OC(=O)C1CCCC(=O)C1
InChI key
WATQNARHYZXAGY-UHFFFAOYSA-N
assay
93%
Application
3-Oxo-1-cyclohexanecarboxylic acid (3-oxocyclohexanecarboxylic acid) may be used in the preparation of 9-(4-chlorobenzoyl)-6-methoxy-2,3,4,9-tetrahydro-1H-carbazole-2-carboxylic acid by reacting with 4-chloro-N-(4-methoxyphenyl)benzohydrazide hydrochloride via Fischer indolization.
General description
3-Oxo-1-cyclohexanecarboxylic acid is a cyclic keto acid that can be prepared starting from 2-acetoxy-1,4-ethoxycarbonylcyclohex-1-ne.
Legal Information
Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Development of potent and selective indomethacin analogues for the inhibition of AKR1C3 (type 5 17?-hydroxysteroid dehydrogenase/prostaglandin F synthase) in castrate-resistant prostate cancer.
Liedtke AJ, et al.
Journal of Medicinal Chemistry, 56(6), 2429-2446 (2013)
2,3-Donor-Acceptor-Substituted 1,3-Butadienes. Synthesis by SO2-extrusion from 3-sulfolenes and diels-alder reactions.
Hoffmann R, et al.
Advanced Synthesis & Catalysis, 336(4), 343-349 (1994)
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