60093-74-5 Usage
Description
(1R,2R)-2-(PROPYLAMINO)CYCLOHEXANOL is a chiral cyclohexanol compound with a molecular formula C9H19NO and a molecular weight of 157.25 g/mol. It belongs to the class of cyclohexanols and features a propylamino group attached to the second carbon of the cyclohexane ring. (1R,2R)-2-(PROPYLAMINO)CYCLOHEXANOL has two stereocenters at the 1 and 2 positions, making it a valuable building block in organic synthesis and pharmaceutical research. Its unique structural features and reactivity contribute to its potential applications in the development of new drugs and as a precursor in the synthesis of other complex molecules.
Uses
Used in Pharmaceutical Research:
(1R,2R)-2-(PROPYLAMINO)CYCLOHEXANOL is used as a building block for the development of new drugs due to its unique structural features and reactivity. Its chiral nature and the presence of the propylamino group make it a promising candidate for the synthesis of various pharmaceutical compounds.
Used in Organic Synthesis:
(1R,2R)-2-(PROPYLAMINO)CYCLOHEXANOL is used as a precursor in the synthesis of other complex molecules. Its versatile structure allows it to be a key component in the creation of a wide range of organic compounds, making it valuable in the field of organic chemistry.
Used in Drug Development:
(1R,2R)-2-(PROPYLAMINO)CYCLOHEXANOL is used as a starting material in the development of new drugs. Its unique properties and reactivity make it a valuable asset in the design and synthesis of innovative pharmaceutical agents, potentially leading to the discovery of novel therapeutics.
Check Digit Verification of cas no
The CAS Registry Mumber 60093-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,9 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60093-74:
(7*6)+(6*0)+(5*0)+(4*9)+(3*3)+(2*7)+(1*4)=105
105 % 10 = 5
So 60093-74-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H19NO/c1-2-7-10-8-5-3-4-6-9(8)11/h8-11H,2-7H2,1H3/t8-,9-/m1/s1
60093-74-5Relevant articles and documents
Asymmetric amination of meso-epoxide with vegetable powder as a low-toxicity catalyst
Asano, Tatsuhiro,Kurata, Hiroyuki,Takeuchi, Yuki,Tsuzaki, Kazuya,Wada, Koichi
, (2020/08/11)
This paper describes the scope and limitation of substrates subjected to asymmetric amination with epoxides catalyzed by a soluble soybean polysaccharide (Soyafibe S-DN), which we recently discovered from the reaction of 1,2-epoxycyclohexane with cyclopropylamine. Various meso-epoxides reacted with various amines afforded the corresponding products with good enantiomeric selectivity. Since it was found that pectin was found to have a catalytic ability after screening commercially available polysaccharides, we studied 33 different vegetable powders having pectic substances, and we found that many vegetable powders showed catalytic ability. These results should guide in using vegetable components as low-toxic catalysts for the production of pharmaceuticals.
Synthesis of β-amino alcohols using MgO as a new catalyst under solvent-free conditions
Hosseini-Sarvari, Mona
, p. 65 - 71 (2008/09/18)
MgO catalyzed efficiently the ring opening of epoxides with a range of aromatic and aliphatic amines to produce β-substituted alcohols in high yields under solvent-free conditions. Exclusive trans stereoselectivity is observed for cyclic epoxide.
