116574-14-2 Usage
Uses
Used in Pharmaceutical Industry:
2-Cyanoacetic acid 1-(diphenylmethyl)-3-azetidinyl ester is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, including the cyano, azetidinyl, and diphenylmethyl groups, allows it to be a key component in the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, 2-Cyanoacetic acid 1-(diphenylmethyl)-3-azetidinyl ester serves as a valuable compound for studying the properties and reactions of esters, cyano groups, and azetidinyl rings. Its complex structure makes it an interesting subject for exploring new reaction pathways and understanding the behavior of similar compounds.
Used in Material Science:
2-Cyanoacetic acid 1-(diphenylmethyl)-3-azetidinyl ester may also find applications in material science, where its unique structural features could be utilized to develop new materials with specific properties. For instance, its potential use in the synthesis of polymers or as a component in the development of advanced materials with tailored characteristics could be explored.
Check Digit Verification of cas no
The CAS Registry Mumber 116574-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,5,7 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116574-14:
(8*1)+(7*1)+(6*6)+(5*5)+(4*7)+(3*4)+(2*1)+(1*4)=122
122 % 10 = 2
So 116574-14-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H18N2O2/c20-12-11-18(22)23-17-13-21(14-17)19(15-7-3-1-4-8-15)16-9-5-2-6-10-16/h1-10,17,19H,11,13-14H2
116574-14-2Relevant academic research and scientific papers
Novel 2-amino-1,4-dihydropyridine calcium antagonists. II. Synthesis and antihypertensive effects of 2-amino-1,4-dihydropyridine derivatives having N,N-dialkylaminoalkoxycarbonyl groups at 3- and/or 5-positions
Kobayashi,Inoue,Nishino,Fujihara,Oizumi,Kimura
, p. 797 - 817 (2007/10/02)
Novel 2-amino-1,4-dihydropyridine derivatives I, which contain N,N-dialkylaminoalkoxycarbonyl groups at the 3- and/or 5-position, were synthesized and their antihypertensive effects were evaluated in spontaneously hypertensive rats. Remarkably prolonged duration of antihypertensive action was observed when a tertiary amino group was introduced into either the 3- or 5-ester side-chain of the 1,4-dihydropyridine ring. In particular, the compounds containing cyclic amino moieties at the 3-position showed greater potency than those with acyclic amino moieties. Chemical modification studies indicated that the two ester side-chains of 1,4-dihydropyridine at the 3- and 5-position might function in a different manner in relation to the antihypertensive activities. 3-(1-Benzhydrylazetidin-3-yl) 5-isopropyl 2-amino-1,4-dihydro-6-methyl-4-(3-nitrophenyl)-3,5-pyridine-dicarboxyl ate, I-43 (CS-905), exhibited potent and long-lasting antihypertensive effects with gradual onset of action, and is a promising candidate as an antihypertensive drug.
