19146-53-3 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-1-Cyclohexylpropan-1-amine is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with improved efficacy and selectivity.
Used in Organic Compounds Synthesis:
(S)-1-Cyclohexylpropan-1-amine is used as an intermediate in the synthesis of other organic compounds, leveraging its unique chemical properties to create a variety of products.
Used in Chiral Building Blocks for Drug Production:
(S)-1-Cyclohexylpropan-1-amine is used as a chiral building block in the production of drugs and agrochemicals, enhancing the enantioselectivity and performance of the final products.
Used in Medical Treatments:
(S)-1-Cyclohexylpropan-1-amine is studied for its potential use in the treatment of various medical conditions, particularly neurological and psychiatric disorders, due to its effects on neurotransmitter systems in the brain.
Used in the Chemical Industry:
(S)-1-Cyclohexylpropan-1-amine is utilized in the chemical industry for its wide range of potential applications, including the development of new materials and processes that benefit from its unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 19146-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,4 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19146-53:
(7*1)+(6*9)+(5*1)+(4*4)+(3*6)+(2*5)+(1*3)=113
113 % 10 = 3
So 19146-53-3 is a valid CAS Registry Number.
19146-53-3Relevant academic research and scientific papers
Preparation of functionalized primary chiral amines and amides via an enantioselective three-component synthesis of propargylamines
Gommermann, Nina,Knochel, Paul
, p. 11418 - 11426 (2007/10/03)
A general preparation of functionalized primary chiral amines and amides from propargylamines has been developed. The chirality is established by an enantioselective three-component reaction of an aldehyde, a terminal alkyne and a secondary amine in the p
Enantioselective synthesis of α,α-disubstituted amines from nitroalkenes
Leroux, Mary-Lorene,Le Gall, Thierry,Mioskowski, Charles
, p. 1817 - 1823 (2007/10/03)
Disubstituted nitroalkenes were converted into enantiomerically enriched amines (isolated as their hydrochloride salts) with enantiometric excesses of 88 to >95% in there steps: (a) highly stereoselective conjugate addition of the potassium salt of 4-phenyloxazolidin-2-one; (b) radical-mediated removal of the nitro group; (c) cleavage of the oxazolidinone.
