Cas 184635-04-9,(R)-1-((S)-2-Benzyloxycarbonylamino-6-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid

184635-04-9

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Basic information

Product Name: (R)-1-((S)-2-Benzyloxycarbonylamino-6-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid
Synonyms: (R)-1-((S)-2-Benzyloxycarbonylamino-6-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid
CAS NO:184635-04-9
Molecular Formula:
Molecular Weight: 463.574
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: (R)-1-((S)-2-Benzyloxycarbonylamino-6-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: (R)-1-((S)-2-Benzyloxycarbonylamino-6-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid(184635-04-9)
EPA Substance Registry System: (R)-1-((S)-2-Benzyloxycarbonylamino-6-tert-butoxycarbonylamino-hexyl)-pyrrolidine-2-carboxylic acid(184635-04-9)

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: 184635-04-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 184635-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,6,3 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 184635-04:
(8*1)+(7*8)+(6*4)+(5*6)+(4*3)+(3*5)+(2*0)+(1*4)=149
149 % 10 = 9
So 184635-04-9 is a valid CAS Registry Number.

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184635-04-9Relevant academic research and scientific papers

Synthesis and antinociceptive activity of some novel nonpeptide derivatives of interleukin-1β (193-195) sequence

Fantetti, Lia,Adembri, Giorgio,Giotti, Alberto,Masini, Ilaria,Roncucci, Gabrio

, p. 137 - 143 (2007/10/03)

The synthesis of a new series of nonpeptide derivatives of interleukin- 1β sequence is described. Compounds have been investigated for their relative activity regarding antinociception and suppression of inflammation. Several compounds with R1(

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