Cas 77280-63-8,{(2-Benzyloxycarbonylamino-acetyl)-[cyclohexylcarbamoyl-(9H-fluoren-9-yl)-methyl]-amino}-acetic acid tert-butyl ester

77280-63-8

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Basic information

Product Name: {(2-Benzyloxycarbonylamino-acetyl)-[cyclohexylcarbamoyl-(9H-fluoren-9-yl)-methyl]-amino}-acetic acid tert-butyl ester
Synonyms: {(2-Benzyloxycarbonylamino-acetyl)-[cyclohexylcarbamoyl-(9H-fluoren-9-yl)-methyl]-amino}-acetic acid tert-butyl ester
CAS NO:77280-63-8
Molecular Formula:
Molecular Weight: 625.765
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: {(2-Benzyloxycarbonylamino-acetyl)-[cyclohexylcarbamoyl-(9H-fluoren-9-yl)-methyl]-amino}-acetic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {(2-Benzyloxycarbonylamino-acetyl)-[cyclohexylcarbamoyl-(9H-fluoren-9-yl)-methyl]-amino}-acetic acid tert-butyl ester(77280-63-8)
EPA Substance Registry System: {(2-Benzyloxycarbonylamino-acetyl)-[cyclohexylcarbamoyl-(9H-fluoren-9-yl)-methyl]-amino}-acetic acid tert-butyl ester(77280-63-8)

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: 77280-63-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 77280-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,8 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77280-63:
(7*7)+(6*7)+(5*2)+(4*8)+(3*0)+(2*6)+(1*3)=148
148 % 10 = 8
So 77280-63-8 is a valid CAS Registry Number.

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77280-63-8Relevant academic research and scientific papers

Aldehyde components for use in four-component condensation ("4CC") Ugi reaction peptide synthesis

Hoyng, Charles F.,Patel, Arvind D.

, p. 4795 - 4798 (1980)

The use of 9-formylfluorene as the aldehyde component in four-component condensation (4CC) fragment strategy peptide synthesis has been investigated in the synthesis of model dipeptides.

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