39884-50-9 Usage
Description
1-(2-Amino-ethyl)-cyclohexanol, also known as 1-amino-2-cyclohexylethanol, is a chemical compound characterized by its molecular formula C8H17NO. It is a colorless or pale yellow liquid with a faint odor and is soluble in water. This versatile compound serves as a building block in the synthesis of various pharmaceuticals and organic compounds, and it is also utilized as a chiral auxiliary in asymmetric synthesis and as a reagent in chemical reactions. Due to its low toxicity and relative safety when handled with proper precautions, it has found a niche in the chemical industry.
Uses
Used in Pharmaceutical Synthesis:
1-(2-Amino-ethyl)-cyclohexanol is used as a building block for the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows for the creation of a wide range of molecules with potential therapeutic applications.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
In the field of asymmetric synthesis, 1-(2-Amino-ethyl)-cyclohexanol is employed as a chiral auxiliary. This application is crucial for the production of enantiomerically pure compounds, which are essential in the pharmaceutical industry to ensure the desired biological activity and minimize potential side effects.
Used as a Reagent in Chemical Reactions:
1-(2-Amino-ethyl)-cyclohexanol also serves as a reagent in various chemical reactions, facilitating the formation of new molecules and contributing to the advancement of chemical research and development.
Used in the Production of Surfactants and Emulsifiers:
1-(2-Amino-ethyl)-cyclohexanol has potential applications in the production of surfactants, emulsifiers, and other specialty chemicals. Its ability to interact with other molecules makes it a valuable component in the formulation of products that require specific properties, such as stability, solubility, or emulsifying capabilities.
Used in the Chemical Industry:
Within the chemical industry, 1-(2-Amino-ethyl)-cyclohexanol is utilized for its diverse applications, including the synthesis of pharmaceuticals, chiral auxiliaries, reagents, and specialty chemicals. Its versatility and low toxicity make it a preferred choice for various chemical processes and product development.
Check Digit Verification of cas no
The CAS Registry Mumber 39884-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,8 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39884-50:
(7*3)+(6*9)+(5*8)+(4*8)+(3*4)+(2*5)+(1*0)=169
169 % 10 = 9
So 39884-50-9 is a valid CAS Registry Number.
39884-50-9Relevant articles and documents
Process for the preparation of N-(2-(cyclo-hexen-1-yl)ethyl)-4-methoxybenzeneacetamide
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, (2008/06/13)
An improved method for preparing a compound having the formula STR1 which is an intermediate in the preparation of dextromethorphan, the improved method comprises the steps of (A) hydrogenating a compound having the formula STR2 in the presence of a hydrogenation catalyst to obtain a compound having the formula STR3 (B) hydrogenating the product of Step (A) in the presence of a hydrogen treated rhodium catalyst to obtain a compound having the formula STR4 (C) reacting the product of Step (B) with 4-methoxyphenylacetic acid to obtain a mixture of compounds comprising STR5 (D) dehydrating the product mixture of Step (C).
Interphenylene 9-thia-11-oxo-12-aza-prostanoic acids
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, (2008/06/13)
This invention relates to novel interphenylene 9-thia-11-oxo-12-azaprostanoic acid compounds, salts, and derivatives thereof. These compounds are exceptionally potent renal vasodilators and antihypertensives which are active when administered orally but which have a more specific type of biological activity than that of many of the natural prostaglandins and their synthetic analogs or derivatives.
