89584-01-0 Usage
Uses
Used in Pharmaceutical Industry:
(1S,2S)-2-Aminocyclohexanol is used as a key intermediate for the synthesis of pharmaceuticals, leveraging its chiral properties to produce enantiopure compounds that are essential in drug development. Its role in creating biologically active molecules contributes to the advancement of new medications and therapies.
Used in Fine Chemicals Production:
In the fine chemicals sector, (1S,2S)-2-Aminocyclohexanol serves as a fundamental building block, facilitating the creation of high-quality specialty chemicals that are used in various applications, including the formulation of high-performance materials and complex chemical compounds.
Used in Agrochemicals Production:
(1S,2S)-2-Aminocyclohexanol is utilized in the production of agrochemicals, where its ability to form biologically active molecules aids in the development of effective crop protection agents and other agricultural products.
Used in Fragrance Industry:
Within the fragrance industry, (1S,2S)-2-Aminocyclohexanol is employed in the synthesis of various scent compounds, contributing to the creation of unique and complex fragrances for a wide range of applications, from perfumes to scented products.
Overall, (1S,2S)-2-Aminocyclohexanol's multifaceted applications across different industries underscore its importance as a versatile and valuable compound in the chemical sector.
Check Digit Verification of cas no
The CAS Registry Mumber 89584-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,8 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89584-01:
(7*8)+(6*9)+(5*5)+(4*8)+(3*4)+(2*0)+(1*1)=180
180 % 10 = 0
So 89584-01-0 is a valid CAS Registry Number.
89584-01-0Relevant articles and documents
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.
SYNTHESIS OF (L)-DAUNOSAMINE AND RELATED AMINO SUGARS
Sammes, Peter G.,Thetford, Dean
, p. 111 - 124 (2007/10/02)
1-(2-Furyl)ethanol (6) has been converted into methyl (+/-)-daunosaminide (1) and methyl (+/-)-ristosaminide (3) by use of an intramolecular cyclisation of a trichloroacetimidate group. (+/-)-Daunosamine (1) has been obtained more directly from the alcohol (10) by use of a modified Mitsunobu reaction; the scope of the latter reaction has been explored using cyclohex-2-en-1-ol as a model substrate.Asymmetric reduction of 2-acetylfuran (5) has given (S)-1-(2-furyl)ethanol (46) in good enantiomeric excess, thus providing a short route to the L-enantiomers of the amino sugars (1), (2), and (3) from a cheap, non-carbohydrate precursor.
NEW ROUTES TO CIS-1,2-HYDROXYAMINES AND RELATED SYSTEMS
Sammes, Peter G.,Thetford, Dean
, p. 2275 - 2278 (2007/10/02)
Use of modified Mitsunobu reactions followed by intramolecular cyclisations have been used to prepare cis-1,2-hydroxyamines, cis-1,3-hydroxyamines, 1,2,3-dihydroxyamines and 1,2,3-diaminoalcohols from allylic alcohols
