Cas 405175-83-9,((R)-2-Benzyloxycarbamoyl-pyrrolidin-1-yl)-(4-methoxy-phenyl)-phosphinic acid ethyl ester

405175-83-9

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Basic information

Product Name: ((R)-2-Benzyloxycarbamoyl-pyrrolidin-1-yl)-(4-methoxy-phenyl)-phosphinic acid ethyl ester
Synonyms: ((R)-2-Benzyloxycarbamoyl-pyrrolidin-1-yl)-(4-methoxy-phenyl)-phosphinic acid ethyl ester
CAS NO:405175-83-9
Molecular Formula:
Molecular Weight: 418.43
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: ((R)-2-Benzyloxycarbamoyl-pyrrolidin-1-yl)-(4-methoxy-phenyl)-phosphinic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((R)-2-Benzyloxycarbamoyl-pyrrolidin-1-yl)-(4-methoxy-phenyl)-phosphinic acid ethyl ester(405175-83-9)
EPA Substance Registry System: ((R)-2-Benzyloxycarbamoyl-pyrrolidin-1-yl)-(4-methoxy-phenyl)-phosphinic acid ethyl ester(405175-83-9)

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: 405175-83-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 405175-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,5,1,7 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 405175-83:
(8*4)+(7*0)+(6*5)+(5*1)+(4*7)+(3*5)+(2*8)+(1*3)=129
129 % 10 = 9
So 405175-83-9 is a valid CAS Registry Number.

405175-83-9Upstream product

362477-53-0 (4-methoxyphenyl)chlorophosphonic acid ethyl ester

405175-83-9Downstream Products

405175-83-9Relevant academic research and scientific papers

New type of metalloproteinase inhibitor: Design and synthesis of new phosphonamide-based hydroxamic acids

Sawa, Masaaki,Kiyoi, Takao,Kurokawa, Kiriko,Kumihara, Hiroshi,Yamamoto, Minoru,Miyasaka, Tomohiro,Ito, Yasuko,Hirayama, Ryoichi,Inoue, Tomomi,Kirii, Yasuyuki,Nishiwaki, Eiji,Ohmoto, Hiroshi,Maeda, Yu,Ishibushi, Etsuko,Inoue, Yoshimasa,Yoshino, Kohichiro,Kondo, Hirosato

, p. 919 - 929 (2007/10/03)

A series of phosphonamide-based hydroxamate derivatives were synthesized, and the inhibitory activities were evaluated against various metalloproteinases in order to clarify its selectivity profile. Among the four diastereomeric isomers resulting from the

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