153922-89-5 Usage
Description
(S)-CYCLOHEX-2-ENYLAMINE, 95%, (98% E.E.) is a cyclohexenylamine, an organic compound with a cyclic structure containing a six-membered ring and an amino group. It is available in a purity of 95% with a 98% enantiomeric excess, making it a valuable compound for specific stereochemical reactions.
Uses
Used in Pharmaceutical Industry:
(S)-CYCLOHEX-2-ENYLAMINE, 95%, (98% E.E.) is used as a chiral building block for the production of pharmaceuticals. Its high enantiomeric excess is particularly useful for reactions that require a specific stereochemical outcome, contributing to the development of more effective and targeted medications.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-CYCLOHEX-2-ENYLAMINE, 95%, (98% E.E.) serves as a key component in the synthesis of various agrochemicals, including pesticides and fertilizers. Its chiral nature allows for the creation of more precise and effective products for agricultural applications.
Used in Research and Development:
(S)-CYCLOHEX-2-ENYLAMINE, 95%, (98% E.E.) is also utilized in the field of medicinal chemistry and drug discovery. It plays a crucial role in research and development, enabling scientists to explore new compounds and potential treatments for various diseases and conditions.
Used in Fine Chemicals Industry:
(S)-CYCLOHEX-2-ENYLAMINE, 95%, (98% E.E.) is also employed in the synthesis of other fine chemicals, which are high-purity chemicals used in various applications, such as fragrances, dyes, and specialty chemicals. The high purity and enantiomeric excess of (S)-CYCLOHEX-2-ENYLAMINE, 95%, (98% E.E.) make it an ideal choice for creating high-quality fine chemicals with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 153922-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,9,2 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 153922-89:
(8*1)+(7*5)+(6*3)+(5*9)+(4*2)+(3*2)+(2*8)+(1*9)=145
145 % 10 = 5
So 153922-89-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H11N/c7-6-4-2-1-3-5-6/h2,4,6H,1,3,5,7H2/p+1/t6-/m1/s1
153922-89-5Relevant articles and documents
Asymmetric Allylic Amination in Water Catalyzed by an Amphiphilic Resin-Supported Chiral Palladium Complex
Uozumi, Yasuhiro,Tanaka, Hirotaka,Shibatomi, Kazutaka
, p. 281 - 283 (2007/10/03)
(Matrix presented) Catalytic asymmetric allylic amination of cycloalkenyl carbonates (methyl cyclohexen-2-yl carbonate, methyl cyclohepten-2-yl carbonate, methyl 5-methoxycarbonylcyclohexen-2-yl carbonate, methyl cyclohexenyl carbonate, tert-butyl 5-methoxycarbonyloxy-1,2,5,6- tetrahydropyridinedicarboxylate) with dibenzylamines ((C6H 5CH2)2NH, (C6H5CH 2)(4-CH3OC6H4CH2)NH, (4-CH3OC6H4CH2)2NH) was achieved in water under heterogeneous conditions by use of a palladium complex of (3R,9aS)-3-[2-(diphenylphosphino)phenyl]-2-phenyltetrahydro-1H-imidazo[1,5-a] indole-1-one anchored on polystyrene-poly(ethylene glycol) copolymer resin to give the corresponding cycloalkenylamines with high enantiomeric selectivity (90-98% ee).