CAS 27489-62-9
:trans-4-Aminocyclohexanol
Description:
Trans-4-Aminocyclohexanol is an organic compound characterized by its cyclohexane ring structure with an amino group and a hydroxyl group attached to the fourth carbon in a trans configuration. This compound is a chiral molecule, meaning it exists in two enantiomeric forms, which can exhibit different biological activities. Trans-4-Aminocyclohexanol is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in water and various organic solvents, making it versatile for different applications. The presence of both the amino and hydroxyl functional groups allows it to participate in hydrogen bonding, influencing its reactivity and interactions with other molecules. This compound is of interest in the fields of medicinal chemistry and materials science, where it may serve as a building block for pharmaceuticals or as a chiral auxiliary in asymmetric synthesis. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C6H13NO
InChI:InChI=1/C6H13NO/c7-5-1-3-6(8)4-2-5/h5-6,8H,1-4,7H2/t5-,6-
InChI key:InChIKey=IMLXLGZJLAOKJN-IZLXSQMJNA-N
SMILES:N[C@H]1CC[C@H](O)CC1
Synonyms:- 1-(1,3-Dioxolan-2-Yl)Methanamine
- 4-Trans Amino Cyclohexanol
- 4-trans-Aminocyclohexanol
- 4-trans-Hydroxycyclohexylamine
- Aminocyclohexanol(Trans-4)
- Aurora Ka-7506
- Cyclohexanol, 4-amino-, trans-
- Timtec-bb sbb005825
- Trans-4-Amino-1-Hydroxycyclohexane
- Trans-4-Aminocyclohexan-1-Ol
- Trans-4-Hydroxycyclohexylamine
- Trans-4-amino cyclohexanol
- trans-1,4-Cyclohexanolamine
- trans-1-Amino-4-cyclohexanol
- trans-1-Amino-4-hydroxycyclohexane
- trans-4-Amino-1-cyclohexanol
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 7 products.
trans-4-Aminocyclohexanol
CAS:Formula:C6H13NOPurity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:115.18trans-4-Aminocyclohexanol, 98+%
CAS:<p>trans-4-Aminocyclohexanol is used as raw material in organic synthesis and is an important intermediate in the synthesis of drugs such as Ambroxol hydrochloride. It can react with butyric acid-(2-chloro-ethyl ester) to get butyric acid 4-amino-cyclohexyl ester. This reaction needs catalytic agent As</p>Formula:C6H13NOPurity:98+%Color and Shape:White to pale cream to pale brown, Crystals or powder or crystalline powder or fused solidMolecular weight:115.18trans-4-Aminocyclohexanol
CAS:Formula:C6H13NOPurity:97%Color and Shape:SolidMolecular weight:115.1735trans-4-Aminocyclohexanol
CAS:trans-4-AminocyclohexanolFormula:C6H13NOPurity:98%Color and Shape: pale yellow solidMolecular weight:115.17g/moltrans-4-Aminocyclohexanol
CAS:<p>Applications trans-4-Aminocyclohexanol, used in the preparation of potential hypertensive agents and other biologically active compounds.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Chan, K.L. et al.: As. J. Pharmacol. Sci., 1, 91 (1979);<br></p>Formula:C6H13NOColor and Shape:NeatMolecular weight:115.174trans-4-Aminocyclohexanol
CAS:<p>Trans-4-aminocyclohexanol is a cell signaling molecule that belongs to the class of heterocyclic compounds. It has been shown to have an anti-inflammatory effect and inhibit the production of pro-inflammatory cytokines in vitro. Trans-4-aminocyclohexanol also inhibits cyclooxygenase (COX) activity, which is responsible for the conversion of arachidonic acid into prostaglandins. This inhibition leads to decreased inflammation and pain. Trans-4-aminocyclohexanol is orally bioavailable and can be detected in the blood plasma within one hour after administration. The compound has been shown to bind to the enzyme protein kinase C, which is involved in cell signaling pathways, and inhibit its activity.</p>Formula:C6H13NOPurity:Min. 95%Color and Shape:PowderMolecular weight:115.17 g/mol






