Basic information Safety Supplier Related

3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96

Basic information Safety Supplier Related

3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96 Basic information

Product Name:
3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96
Synonyms:
  • 3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96
  • 3-oxo-cyclohexanecarboxylic acid
  • 3-Ketocyclohexyl carboxylate
  • 3-Carboxycyclohexan-1-one
  • 3-oxocyclohexanecarboxylate
  • Cyclohexanecarboxylic acid, 3-oxo-
  • 1-Carboxy-3-oxocyclohexane
  • O**3-OXO-1-CYCLOHEXANECARBOXYLIC ACID
CAS:
16205-98-4
MF:
C7H10O3
MW:
142.15
Product Categories:
  • Carboxylic Acids
  • Carboxylic Acids
  • Ring Systems
  • C7
  • Carbonyl Compounds
Mol File:
16205-98-4.mol
More
Less

3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96 Chemical Properties

Melting point:
76 °C
Boiling point:
309.7±35.0 °C(Predicted)
Density 
1.233±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
4.72±0.20(Predicted)
color 
White
InChI
InChI=1S/C7H10O3/c8-6-3-1-2-5(4-6)7(9)10/h5H,1-4H2,(H,9,10)
InChIKey
WATQNARHYZXAGY-UHFFFAOYSA-N
SMILES
C1(C(O)=O)CCCC(=O)C1
More
Less

Safety Information

WGK Germany 
3
HS Code 
2918300090
More
Less

3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96 Usage And Synthesis

Uses

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.

Synthesis

606488-94-2

16205-98-4

Preparation of Jones oxidizing reagent: Jones reagent was prepared by mixing sulfuric acid (30 mL), CrO3 (8.1 g) and H2O (30 mL) under ice/water bath conditions. The prepared Jones reagent was slowly added dropwise to a solution of 3-hydroxycyclohexane-1-carboxylic acid (11 g, 76.3 mmol, 1.00 eq.) in acetone (150 mL) over 30 min at 0 °C. After the dropwise addition was completed, the reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the solid impurities were removed by filtration. The filtrate was extracted with dichloromethane (3 x 100 mL). The organic layers were combined, washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the crude 3-oxocyclohexane-1-carboxylic acid (8.7 g) as a yellow oil.

References

[1] Patent: WO2014/11902, 2014, A1. Location in patent: Paragraph 00282-00283
[2] Patent: WO2014/194242, 2014, A2. Location in patent: Paragraph 00353; 00355

3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96Supplier

Taizhou Elitechemie MediPharma Technology Co., Ltd. Gold
Tel
523-86810021 18921709486
Email
gwli@elitechemie.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Email
isenchem@163.com
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Email
chenyj@titansci.com
Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Email
sales@accelachem.com