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CIS-3-AMINO-CYCLOHEXANOL HYDROCHLORIDE, also known as (1S,3R)-3-Aminocyclohexanol Hydrochloride, is an organic compound that serves as a key reactant in the synthesis of pharmaceutical compounds. It is characterized by its unique cyclohexanol structure with an amino group at the 3-position and a hydrochloride counterion, which contributes to its reactivity and potential applications in medicinal chemistry.

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  • 124555-44-8 Structure
  • Basic information

    1. Product Name: CIS-3-AMINO-CYCLOHEXANOL HYDROCHLORIDE
    2. Synonyms: CIS-3-AMINO-CYCLOHEXANOL HYDROCHLORIDE;(1S,3R)-3-Amino-cyclohexanol hydrochloride;(1S,3R)-3-aminocyclohexan-1-ol
    3. CAS NO:124555-44-8
    4. Molecular Formula: C6H13NO*ClH
    5. Molecular Weight: 151.636
    6. EINECS: N/A
    7. Product Categories: organic building block
    8. Mol File: 124555-44-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Refrigerator, Under Inert Atmosphere
    8. Solubility: Methanol (Slightly), Water (Slightly)
    9. CAS DataBase Reference: CIS-3-AMINO-CYCLOHEXANOL HYDROCHLORIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: CIS-3-AMINO-CYCLOHEXANOL HYDROCHLORIDE(124555-44-8)
    11. EPA Substance Registry System: CIS-3-AMINO-CYCLOHEXANOL HYDROCHLORIDE(124555-44-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 124555-44-8(Hazardous Substances Data)

124555-44-8 Usage

Uses

Used in Pharmaceutical Industry:
CIS-3-AMINO-CYCLOHEXANOL HYDROCHLORIDE is used as a reactant for the preparation of isoxazole carboxamide compounds. These compounds are potent, soluble, and orally active TRPV1 antagonists and analgesics, making them valuable in the development of new pain management therapies.
In the synthesis of isoxazole carboxamide compounds, CIS-3-AMINO-CYCLOHEXANOL HYDROCHLORIDE plays a crucial role in the formation of the desired molecular structure, which is essential for the biological activity and therapeutic potential of the final product. By incorporating this compound into the synthesis process, researchers can create novel and effective treatments for various types of pain, potentially improving patient outcomes and quality of life.

Check Digit Verification of cas no

The CAS Registry Mumber 124555-44-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,5 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 124555-44:
(8*1)+(7*2)+(6*4)+(5*5)+(4*5)+(3*5)+(2*4)+(1*4)=118
118 % 10 = 8
So 124555-44-8 is a valid CAS Registry Number.

124555-44-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,3S)-3-aminocyclohexan-1-ol,hydrochloride

1.2 Other means of identification

Product number -
Other names (+-)-cis-3-amino-cyclohexanol,hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:124555-44-8 SDS

124555-44-8Downstream Products

124555-44-8Relevant articles and documents

TETRACYCLIC HETEROCYCLE COMPOUNDS USEFUL AS HIV INTEGRASE INHIBITORS

-

Page/Page column 34; 35, (2015/04/15)

The present invention relates to Tetracyclic Heterocycle Compounds of Formula (I) and pharmaceutically acceptable salts or prodrug thereof, wherein n, X, Y, Z, R1, R2, and R3 are as defined herein. The present invention also relates to compositions comprising at least one Tetracyclic Heterocycle Compound, and methods of using the Tetracyclic Heterocycle Compounds for treating or preventing HIV infection in a subject.

Stereocontrolled Preparation of Cyclohexane Amino Alcohols Utilising a Modified Mitsunobu Reaction

Sammes, Peter G.,Thetford, Dean

, p. 655 - 661 (2007/10/02)

A method for the introduction of amino groups into aliphatic systems is described.Cyclohex-2-enol reacts with aromatic diacylamines under Mitsunobu reaction conditions to give either N-alkylated or O-alkylated products in a controlled, predictable manner.

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