Cas 160036-37-3,(S)-2-{(S)-2-[2-(9H-Fluoren-9-ylmethoxycarbonylamino)-acetylamino]-3-phenyl-propionylamino}-4-methyl-pentanoic acid pentafluorophenyl ester

160036-37-3

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Basic information

Product Name: (S)-2-{(S)-2-[2-(9H-Fluoren-9-ylmethoxycarbonylamino)-acetylamino]-3-phenyl-propionylamino}-4-methyl-pentanoic acid pentafluorophenyl ester
Synonyms:
CAS NO:160036-37-3
Molecular Formula:
Molecular Weight: 723.696
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: (S)-2-{(S)-2-[2-(9H-Fluoren-9-ylmethoxycarbonylamino)-acetylamino]-3-phenyl-propionylamino}-4-methyl-pentanoic acid pentafluorophenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-{(S)-2-[2-(9H-Fluoren-9-ylmethoxycarbonylamino)-acetylamino]-3-phenyl-propionylamino}-4-methyl-pentanoic acid pentafluorophenyl ester(160036-37-3)
EPA Substance Registry System: (S)-2-{(S)-2-[2-(9H-Fluoren-9-ylmethoxycarbonylamino)-acetylamino]-3-phenyl-propionylamino}-4-methyl-pentanoic acid pentafluorophenyl ester(160036-37-3)

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: 160036-37-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 160036-37-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,0,3 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 160036-37:
(8*1)+(7*6)+(6*0)+(5*0)+(4*3)+(3*6)+(2*3)+(1*7)=93
93 % 10 = 3
So 160036-37-3 is a valid CAS Registry Number.

160036-37-3Upstream product

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160036-37-3Relevant academic research and scientific papers

Synthesis of peptide derivatives of 5-fluorouracil

Nichifor, Marieta,Schacht, Etienne H.

, p. 3747 - 3760 (1994)

The preparation of di-, tetra- and pentapeptides carrying 5-fluorouracil as an α-substituent of a terminal glycine moiety is described. The dipeptide compounds were synthetized by addition of ethyl glyoxylate to N-(benzyl-oxycarbonyl)-amino acid amides, s

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