Cas 176041-72-8,(S)-2-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-propionylamino]-3-phenyl-propionic acid 2,2-dichloro-cyclopropyl ester

176041-72-8

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Basic information

Product Name: (S)-2-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-propionylamino]-3-phenyl-propionic acid 2,2-dichloro-cyclopropyl ester
Synonyms:
CAS NO:176041-72-8
Molecular Formula:
Molecular Weight: 516.422
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: (S)-2-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-propionylamino]-3-phenyl-propionic acid 2,2-dichloro-cyclopropyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-propionylamino]-3-phenyl-propionic acid 2,2-dichloro-cyclopropyl ester(176041-72-8)
EPA Substance Registry System: (S)-2-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-propionylamino]-3-phenyl-propionic acid 2,2-dichloro-cyclopropyl ester(176041-72-8)

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: 176041-72-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 176041-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,0,4 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 176041-72:
(8*1)+(7*7)+(6*6)+(5*0)+(4*4)+(3*1)+(2*7)+(1*2)=128
128 % 10 = 8
So 176041-72-8 is a valid CAS Registry Number.

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176041-72-8Relevant academic research and scientific papers

Mechanism-based inactivation of α-chymotrypsin

Ohba, Tsuyoshi,Tsuchiya, Naoki,Nishimura, Kuniko,Ikeda, Eitatsu,Wakayama, Jun,Takei, Hisashi

, p. 543 - 546 (2007/10/03)

The peptidyl ester derivatives of 2,2-dichlorocyclopropanol and the amide derivative of 2,2-dichlorocyclopropylamine were prepared as novel mechanism-based inactivators of α-chymotrypsin. The esters inactivated α-chymotrypsin irreversibly but the amide did not show any irreversible inhibitory activity toward α-chymotrypsin.

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