Cas 222853-58-9,N'-(2-tert-butoxycarbonylamino-3-phenyl-propionyl)-N-(2-carbamoyl-ethyl)-hydrazinecarboxylic acid 2,2,2-trichloro-ethyl ester

222853-58-9

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Basic information

Product Name: N'-(2-tert-butoxycarbonylamino-3-phenyl-propionyl)-N-(2-carbamoyl-ethyl)-hydrazinecarboxylic acid 2,2,2-trichloro-ethyl ester
Synonyms: N'-(2-tert-butoxycarbonylamino-3-phenyl-propionyl)-N-(2-carbamoyl-ethyl)-hydrazinecarboxylic acid 2,2,2-trichloro-ethyl ester
CAS NO:222853-58-9
Molecular Formula:
Molecular Weight: 525.817
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'-(2-tert-butoxycarbonylamino-3-phenyl-propionyl)-N-(2-carbamoyl-ethyl)-hydrazinecarboxylic acid 2,2,2-trichloro-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N'-(2-tert-butoxycarbonylamino-3-phenyl-propionyl)-N-(2-carbamoyl-ethyl)-hydrazinecarboxylic acid 2,2,2-trichloro-ethyl ester(222853-58-9)
EPA Substance Registry System: N'-(2-tert-butoxycarbonylamino-3-phenyl-propionyl)-N-(2-carbamoyl-ethyl)-hydrazinecarboxylic acid 2,2,2-trichloro-ethyl ester(222853-58-9)

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: 222853-58-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 222853-58-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,8,5 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 222853-58:
(8*2)+(7*2)+(6*2)+(5*8)+(4*5)+(3*3)+(2*5)+(1*8)=129
129 % 10 = 9
So 222853-58-9 is a valid CAS Registry Number.

222853-58-9Upstream product

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222853-58-9Relevant academic research and scientific papers

Design, synthesis, and evaluation of azapeptides as substrates and inhibitors for human rhinovirus 3C protease

Venkatraman, Shankar,Kong, Jian-she,Nimkar, Sanjay,Wang, Q. May,Aube, Jeffrey,Hanzlik, Robert P.

, p. 577 - 580 (2007/10/03)

A series of azapeptides was prepared and assessed as inhibitors of the human rhinovirus 3C protease. Boc-VLFaQ-OPh was a slow-turnover substrate that gave transient (ca. 1-2 h) inhibition as it underwent hydrolysis. Boc- VLFaG-OPh gave very slow but essen

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