Cas 870822-63-2,N-{[(9H-fluoren-9-yl)methoxy][2-(4-trifluoromethylphenyl)ethyl]phosphinyl}-L-glutamic acid dimethyl ester

870822-63-2

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Basic information

Product Name: N-{[(9H-fluoren-9-yl)methoxy][2-(4-trifluoromethylphenyl)ethyl]phosphinyl}-L-glutamic acid dimethyl ester
Synonyms:
CAS NO:870822-63-2
Molecular Formula:
Molecular Weight: 589.548
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: N-{[(9H-fluoren-9-yl)methoxy][2-(4-trifluoromethylphenyl)ethyl]phosphinyl}-L-glutamic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N-{[(9H-fluoren-9-yl)methoxy][2-(4-trifluoromethylphenyl)ethyl]phosphinyl}-L-glutamic acid dimethyl ester(870822-63-2)
EPA Substance Registry System: N-{[(9H-fluoren-9-yl)methoxy][2-(4-trifluoromethylphenyl)ethyl]phosphinyl}-L-glutamic acid dimethyl ester(870822-63-2)

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: 870822-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 870822-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,8,2 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 870822-63:
(8*8)+(7*7)+(6*0)+(5*8)+(4*2)+(3*2)+(2*6)+(1*3)=182
182 % 10 = 2
So 870822-63-2 is a valid CAS Registry Number.

870822-63-2Upstream product

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870822-63-2Relevant academic research and scientific papers

Optimizing phenylethylphosphonamidates for the inhibition of prostate-specific membrane antigen

Wone, David W.G.,Rowley, Jennifer A.,Garofalo, Albert W.,Berkman, Clifford E.

, p. 67 - 76 (2007/10/03)

A series of eight N-2-phenylethylphosphonyl derivatives of glutamic acid was prepared to determine if the inhibitory potency of a phenylethylphosphonyl derivative of glutamic acid against prostate-specific membrane antigen (PSMA) could be improved through

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