(1R,3S)
(1R,3S)-3-Aminocyclohexanol
CAS: 1110772-22-9
Molecular Formula: C6H13NO
(1R,3S) - Names and Identifiers
| Name | (1R,3S)-3-Aminocyclohexanol |
| Synonyms | (1R,3S) (1R,3S)-3-AMINOCYCLOHEXANOL (1R,3S)-3-Aminocyclohexanol (1R,3S)-3-aminocyclohexan-1-ol Cyclohexanol, 3-amino-, (1R,3S)- Cis-(1R,3S)-3-aMino-cyclohexanol hydrochloride |
| CAS | 1110772-22-9 |
| InChI | InChI=1S/C6H13NO/c7-5-2-1-3-6(8)4-5/h5-6,8H,1-4,7H2/t5-,6+/m0/s1 |
(1R,3S) - Physico-chemical Properties
| Molecular Formula | C6H13NO |
| Molar Mass | 115.17 |
| Density | 1.037±0.06 g/cm3(Predicted) |
| Boling Point | 201.1±33.0 °C(Predicted) |
| pKa | 15.09±0.40(Predicted) |
| Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
(1R,3S) - Introduction
(1R,3S)-3-aminocyclohexanol is a chiral organic compound with the formula C6H13NO. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
(1R,3S)-3-aminocyclohexanol is a solid, and its appearance is white crystal or powder. It has two chiral centers, so there are four possible stereoisomers. Its optical rotation is positive and its optical rotation is 10.2 °(c = 1, ethanol). The compound is sparingly soluble in water and soluble in ethanol and other organic solvents.
Use:
(1R,3S)-3-aminocyclohexanol is widely used in the field of medicine. As a chiral intermediate, it is often used in the preparation of active forms of drugs in the synthesis of drugs. It is also used for the preparation of aminocyclohexane-containing compounds which have important applications in the agrochemical and pharmaceutical fields.
Preparation Method:
The preparation method of (1R,3S)-3-aminocyclohexanol can be achieved through various routes. A common method is to use 1,2-cyclohexanediol acetate chloride to obtain (1R,3S)-3-aminocyclohexanol by reduction. In this process, the hydroxyl moiety is substituted with an amino group.
Safety Information:
Nature:
(1R,3S)-3-aminocyclohexanol is a solid, and its appearance is white crystal or powder. It has two chiral centers, so there are four possible stereoisomers. Its optical rotation is positive and its optical rotation is 10.2 °(c = 1, ethanol). The compound is sparingly soluble in water and soluble in ethanol and other organic solvents.
Use:
(1R,3S)-3-aminocyclohexanol is widely used in the field of medicine. As a chiral intermediate, it is often used in the preparation of active forms of drugs in the synthesis of drugs. It is also used for the preparation of aminocyclohexane-containing compounds which have important applications in the agrochemical and pharmaceutical fields.
Preparation Method:
The preparation method of (1R,3S)-3-aminocyclohexanol can be achieved through various routes. A common method is to use 1,2-cyclohexanediol acetate chloride to obtain (1R,3S)-3-aminocyclohexanol by reduction. In this process, the hydroxyl moiety is substituted with an amino group.
Safety Information:
Last Update：2024-04-09 20:49:11
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View History
(1R,3S)
466-99-9
68803-79-2
carbon
10340-91-7
104-68-7
2-methyloxazoline
beta-hydroxy-1-ethylaziridine
Fluorescent Brightener OB-1
2-Hydroxymethylbenzothiazole
466-99-9
68803-79-2
carbon
10340-91-7
104-68-7
2-methyloxazoline
beta-hydroxy-1-ethylaziridine
Fluorescent Brightener OB-1
2-Hydroxymethylbenzothiazole