16037-15-3 Usage
Description
L-PROLINE BETA-NAPHTHYLAMIDE HYDROCHLORIDE is an L-proline derivative that is formed by the formal condensation of the carboxy group of L-proline with the amino group of 2-naphthylamine. L-PROLINE BETA-NAPHTHYLAMIDE HYDROCHLORIDE is a chemical entity with potential applications in various fields due to its unique structure and properties.
Uses
Used in Pharmaceutical Industry:
L-PROLINE BETA-NAPHTHYLAMIDE HYDROCHLORIDE is used as a pharmaceutical compound for its potential therapeutic applications. The specific application reason is not provided in the materials, but given its structure as an L-proline derivative, it may have implications in the development of new drugs or drug candidates targeting various diseases.
Used in Chemical Research:
L-PROLINE BETA-NAPHTHYLAMIDE HYDROCHLORIDE is used as a research compound for studying its chemical properties, interactions, and potential applications in chemical synthesis. The compound's unique structure may provide insights into the development of new chemical reactions or the modification of existing ones.
Please note that the provided materials do not specify any particular use for L-PROLINE BETA-NAPHTHYLAMIDE HYDROCHLORIDE, so the applications listed above are inferred based on its structure and the general uses of similar compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 16037-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,3 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16037-15:
(7*1)+(6*6)+(5*0)+(4*3)+(3*7)+(2*1)+(1*5)=83
83 % 10 = 3
So 16037-15-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H16N2O/c18-15(14-6-3-9-16-14)17-13-8-7-11-4-1-2-5-12(11)10-13/h1-2,4-5,7-8,10,14,16H,3,6,9H2,(H,17,18)/t14-/m0/s1
16037-15-3Relevant articles and documents
Chiral lewis base catalyzed highly enantioselective reduction of N-alkyl β-enamino esters with trichlorosilane and water
Wu, Xinjun,Li, Yang,Wang, Chao,Zhou, Li,Lu, Xiaoxia,Sun, Jian
, p. 2846 - 2848 (2011/04/24)
First, test the water! In the presence of a chiral Lewis base catalyst 2, the supposedly moisture-unfriendly reduction system with trichlorosilane was found to be highly efficient and enantioselective when using water as an additive. For the first time, this method enables the reduction of a broad range of N-alkyl β-enamino esters 1 to give N-alkyl β-amino esters 3 in good to high yields and with excellent enantioselectivities (see scheme).
