2-Aminocyclohexanol
2-Aminocyclohexanol Basic information
- Product Name:
- 2-Aminocyclohexanol
- Synonyms:
-
- aminocyclohexanol
- 2-Aminocyclohenxanol
- 2-Aminocyclohexanol 98%
- 2-Aminocyclohexanol98%
- 1-Amino-2-hydroxycyclohexane
- 2-Aminocyclohexanol (cis- and trans- mixture)
- 2-Aminocyclohexanol
- 2-Aminocyclohexan-1-ol 98%
- CAS:
- 6850-38-0
- MF:
- C6H13NO
- MW:
- 115.17
- Mol File:
- 6850-38-0.mol
2-Aminocyclohexanol Chemical Properties
- Melting point:
- 65 °C
- Boiling point:
- 212 °C
- Density
- 1.037±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- solubility
- soluble in Methanol
- form
- powder to crystal
- pka
- 14.94±0.40(Predicted)
- color
- White to Light orange to Yellow
- InChIKey
- PQMCFTMVQORYJC-UHFFFAOYSA-N
- CAS DataBase Reference
- 6850-38-0(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,Xn
- Risk Statements
- 34-22
- Safety Statements
- 26-36/37/39
- RIDADR
- 3259
- Hazard Note
- Irritant
- HazardClass
- 8
- PackingGroup
- III
- HS Code
- 2922190090
2-Aminocyclohexanol Usage And Synthesis
Chemical Properties
White to Light orange to Yellow powder to crystal.
Uses
Trans-2-aminocyclohexanol and cis-/trans-1,2-cyclohexanediamines have found their application in the synthesis of the antiarrhythmic medicament vernakalant and spleen tyrosine kinase inhibitor, κ-opioid analgesics.
Preparation
2-Aminocyclohexanol Synthesis: Under water bath reaction conditions, 214.3 g of ammonia water was added to a 500 mL three-necked flask. Stir and heat, and when the internal temperature reaches about 50°C, start to slowly drop 50.0 g of 1,2-epoxycyclohexane into the reaction flask. After the dropwise addition was completed, the reaction was performed at a constant temperature for 12h. After the reaction was completed, the reaction was processed to obtain a crude product, which was purified by recrystallization to obtain 2-aminocyclohexanol with a yield of 90% and an amine value (mgKOH/g) of 453.
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2-Aminocyclohexanol(6850-38-0)Related Product Information
- EC 2.6.1.2
- Cyclohexanone
- Tris(hydroxymethyl)aminomethane
- Acetaminophen
- Cyclohexanol
- Molasses
- SPECTINOMYCIN DIHYDROCHLORIDE
- RIBOSTAMYCIN SULFATE SALT
- (1'R,3'S,3S,5R,6R)-5-AMINO-2-AMINOMETHYL-6-(4,6-DIAMINO-2,3-DIHYDROXY-CYCLOHEXYLOXY)-TETRAHYDRO-PYRAN-3,4-DIOL
- Sisomicin
- TRANS-2-AMINOCYCLOHEXANOL HYDROCHLORIDE
- Amino alcohol
- trans-4-Aminocyclohexanol
- Neomycin sulfate
- KANAMYCIN
- Gentamicin
- Spectinomycin
- 4-Aminocyclohexanol