Cas 222610-57-3,tris<4-(S)-(2-methoxycarbonyl-2-acetamidoethyl)phenyl> phosphite

222610-57-3

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Basic information

Product Name: tris<4-(S)-(2-methoxycarbonyl-2-acetamidoethyl)phenyl> phosphite
Synonyms: tris<4-(S)-(2-methoxycarbonyl-2-acetamidoethyl)phenyl> phosphite
CAS NO:222610-57-3
Molecular Formula:
Molecular Weight: 739.716
EINECS: N/A
Product Categories: N/A
Mol File: 222610-57-3.mol
Article Data: 1

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: tris<4-(S)-(2-methoxycarbonyl-2-acetamidoethyl)phenyl> phosphite(CAS DataBase Reference)
NIST Chemistry Reference: tris<4-(S)-(2-methoxycarbonyl-2-acetamidoethyl)phenyl> phosphite(222610-57-3)
EPA Substance Registry System: tris<4-(S)-(2-methoxycarbonyl-2-acetamidoethyl)phenyl> phosphite(222610-57-3)

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: 222610-57-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 222610-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,6,1 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 222610-57:
(8*2)+(7*2)+(6*2)+(5*6)+(4*1)+(3*0)+(2*5)+(1*7)=93
93 % 10 = 3
So 222610-57-3 is a valid CAS Registry Number.

222610-57-3Upstream product

2440-79-1 N-acetyl-L-tyrosine methyl ester

222610-57-3Downstream Products

222610-57-3Relevant articles and documents

Structure-activity relationship of diaryl phosphonate esters as potent irreversible dipeptidyl peptidase IV inhibitors.

Belayev, Alexander,Zhang, Xuemei,Augustyns, Koen,Lambeir, Anne-Marie,Meester, Ingrid De,et al.

, p. 1041 - 1052 (2007/10/03)

The previously reported diphenyl 1-(S)-prolylpyrrolidine-2(R, S)-phosphonate (5) was used as a lead compound for the development of potent and irreversible inhibitors of dipeptidyl peptidase IV (DPP IV, EC 3.4.14.5). The synthesis of a series of diaryl 1-

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