Cas 903528-95-0,[(1-chlorocarbonyl-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid 9<i>H</i>-fluoren-9-ylmethyl ester

903528-95-0

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Basic information

Product Name: [(1-chlorocarbonyl-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid 9H-fluoren-9-ylmethyl ester
Synonyms: [(1-chlorocarbonyl-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid 9H-fluoren-9-ylmethyl ester
CAS NO:903528-95-0
Molecular Formula:
Molecular Weight: 462.933
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: [(1-chlorocarbonyl-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid 9H-fluoren-9-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(1-chlorocarbonyl-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid 9H-fluoren-9-ylmethyl ester(903528-95-0)
EPA Substance Registry System: [(1-chlorocarbonyl-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid 9H-fluoren-9-ylmethyl ester(903528-95-0)

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: 903528-95-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 903528-95-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,3,5,2 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 903528-95:
(8*9)+(7*0)+(6*3)+(5*5)+(4*2)+(3*8)+(2*9)+(1*5)=170
170 % 10 = 0
So 903528-95-0 is a valid CAS Registry Number.

903528-95-0Upstream product

117370-45-3 (9-fluorenylmethyloxycarbonyl)glycyl-L-phenylalanine

903528-95-0Downstream Products

903528-95-0Relevant academic research and scientific papers

Nα-Fmoc-peptide azides: Synthesis, isolation, characterization and utility in the extension of peptide chains

Suresh Babu, Vommina V.,Vasanthakumar, Ganga-Ramu,Patil, Basanagoud S.

, p. 1853 - 1858 (2007/10/03)

Syntheses of Nα-Fmoc-peptide azides employing acid chloride as well as mixed anhydride methods have been carried out. The resulting Fmoc-peptide azides prepared have been isolated as solids in good yield (75-92 %) and are found to be analytical

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