Cas 84866-25-1,N-carbobenzoxy(imbutyloxycarbonyl)-His-(O-tert-butyl)-Asp-(O-tert-butyl)-Ser-Gly-pentachlorophenyl ester

84866-25-1

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Basic information

Product Name: N-carbobenzoxy(imbutyloxycarbonyl)-His-(O-tert-butyl)-Asp-(O-tert-butyl)-Ser-Gly-pentachlorophenyl ester
Synonyms: N-carbobenzoxy(imbutyloxycarbonyl)-His-(O-tert-butyl)-Asp-(O-tert-butyl)-Ser-Gly-pentachlorophenyl ester
CAS NO:84866-25-1
Molecular Formula:
Molecular Weight: 1009.16
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: N-carbobenzoxy(imbutyloxycarbonyl)-His-(O-tert-butyl)-Asp-(O-tert-butyl)-Ser-Gly-pentachlorophenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N-carbobenzoxy(imbutyloxycarbonyl)-His-(O-tert-butyl)-Asp-(O-tert-butyl)-Ser-Gly-pentachlorophenyl ester(84866-25-1)
EPA Substance Registry System: N-carbobenzoxy(imbutyloxycarbonyl)-His-(O-tert-butyl)-Asp-(O-tert-butyl)-Ser-Gly-pentachlorophenyl ester(84866-25-1)

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: 84866-25-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 84866-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,6 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84866-25:
(7*8)+(6*4)+(5*8)+(4*6)+(3*6)+(2*2)+(1*5)=171
171 % 10 = 1
So 84866-25-1 is a valid CAS Registry Number.

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84866-25-1Relevant academic research and scientific papers

Synthesis and catalytic activity of Poly-L-Histidyl-L-Aspartyl-L-Seryl-Glycine

Sarwal,Adigun,Stephani,Kapoor

, p. 1380 - 1383 (2007/10/02)

Poly(His-Asp-Ser-Gly) was synthesized from the fully protected tetrapeptide active ester hydrochloride, which was prepared by stepwise coupling, using pentachlorophenyl ester and mixed anhydride methods. Complete deprotection of the protected tetrapeptide

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