Cas 75957-50-5,Carbamic acid, [1-methyl-2-[(4-methyl-2-oxo-2H-1-benzopyran-7-yl)amino]-2-oxoethyl]-, phenylmethyl ester, (S)-

75957-50-5

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Basic information

Product Name: Carbamic acid, [1-methyl-2-[(4-methyl-2-oxo-2H-1-benzopyran-7-yl)amino]-2-oxoethyl]-, phenylmethyl ester, (S)-
Synonyms:
CAS NO:75957-50-5
Molecular Formula: C21H20N2O5
Molecular Weight: 380.4
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Carbamic acid, [1-methyl-2-[(4-methyl-2-oxo-2H-1-benzopyran-7-yl)amino]-2-oxoethyl]-, phenylmethyl ester, (S)-(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [1-methyl-2-[(4-methyl-2-oxo-2H-1-benzopyran-7-yl)amino]-2-oxoethyl]-, phenylmethyl ester, (S)-(75957-50-5)
EPA Substance Registry System: Carbamic acid, [1-methyl-2-[(4-methyl-2-oxo-2H-1-benzopyran-7-yl)amino]-2-oxoethyl]-, phenylmethyl ester, (S)-(75957-50-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 75957-50-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 75957-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,5 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75957-50:
(7*7)+(6*5)+(5*9)+(4*5)+(3*7)+(2*5)+(1*0)=175
175 % 10 = 5
So 75957-50-5 is a valid CAS Registry Number.

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75957-50-5Relevant academic research and scientific papers

Synthesis and carbonic anhydrase inhibitory properties of amino acid – coumarin/quinolinone conjugates incorporating glycine, alanine and phenylalanine moieties

Kü?ükbay, F. Zehra,Kü?ükbay, Hasan,Tanc, Muhammet,Supuran, Claudiu T.

, p. 1198 - 1202 (2016)

N-Protected amino acids (Gly, Ala and Phe) were reacted with amino substituted coumarin and quinolinone derivatives, leading to the corresponding N-protected amino acid–coumarin/quinolinone conjugates. The carbonic anhydrase (CA, EC 4.2.1.1) inhibitory ac

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