Cas 262279-53-8,(S)-6-(Diethoxy-phosphoryl)-6,6-difluoro-5-oxo-2-(trityl-amino)-hexanoic acid methyl ester

262279-53-8

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Basic information

Product Name: (S)-6-(Diethoxy-phosphoryl)-6,6-difluoro-5-oxo-2-(trityl-amino)-hexanoic acid methyl ester
Synonyms: (S)-6-(Diethoxy-phosphoryl)-6,6-difluoro-5-oxo-2-(trityl-amino)-hexanoic acid methyl ester
CAS NO:262279-53-8
Molecular Formula:
Molecular Weight: 573.574
EINECS: N/A
Product Categories: N/A
Mol File: 262279-53-8.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: (S)-6-(Diethoxy-phosphoryl)-6,6-difluoro-5-oxo-2-(trityl-amino)-hexanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-6-(Diethoxy-phosphoryl)-6,6-difluoro-5-oxo-2-(trityl-amino)-hexanoic acid methyl ester(262279-53-8)
EPA Substance Registry System: (S)-6-(Diethoxy-phosphoryl)-6,6-difluoro-5-oxo-2-(trityl-amino)-hexanoic acid methyl ester(262279-53-8)

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: 262279-53-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 262279-53-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,2,2,7 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 262279-53:
(8*2)+(7*6)+(6*2)+(5*2)+(4*7)+(3*9)+(2*5)+(1*3)=148
148 % 10 = 8
So 262279-53-8 is a valid CAS Registry Number.

262279-53-8Upstream product

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262279-53-8Relevant articles and documents

Synthesis and characterization of intermediate and transition-state analogue inhibitors of γ-gutamyl peptide ligases

Inoue, Makoto,Hiratake, Jun,Sakata, Kanzo

, p. 2248 - 2251 (1999)

The phosphonodifluoromethyl ketone and phosphonofluoridate derivatives of L-glutamic acid were synthesized and characterized as analogues of the γ-glutamyl phosphate intermediate and the tetrahedral transition state, respectively, for the inhibition of γ-

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