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.
124555-44-8Relevant articles and documents
TETRACYCLIC HETEROCYCLE COMPOUNDS USEFUL AS HIV INTEGRASE INHIBITORS
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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.