Cas 577793-31-8,2-{5-[(6-<i>tert</i>-butoxycarbonylamino-2-methyl-pyridin-3-ylmethyl)-carbamoyl]-1,3-dioxo-5,8-dihydro-[1,2,4]triazolo[1,2-<i>a</i>]pyridazin-2-yl}-acrylic acid cyclohexyl ester

577793-31-8

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Basic information

Product Name: 2-{5-[(6-tert-butoxycarbonylamino-2-methyl-pyridin-3-ylmethyl)-carbamoyl]-1,3-dioxo-5,8-dihydro-[1,2,4]triazolo[1,2-a]pyridazin-2-yl}-acrylic acid cyclohexyl ester
Synonyms:
CAS NO:577793-31-8
Molecular Formula:
Molecular Weight: 568.63
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: 2-{5-[(6-tert-butoxycarbonylamino-2-methyl-pyridin-3-ylmethyl)-carbamoyl]-1,3-dioxo-5,8-dihydro-[1,2,4]triazolo[1,2-a]pyridazin-2-yl}-acrylic acid cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-{5-[(6-tert-butoxycarbonylamino-2-methyl-pyridin-3-ylmethyl)-carbamoyl]-1,3-dioxo-5,8-dihydro-[1,2,4]triazolo[1,2-a]pyridazin-2-yl}-acrylic acid cyclohexyl ester(577793-31-8)
EPA Substance Registry System: 2-{5-[(6-tert-butoxycarbonylamino-2-methyl-pyridin-3-ylmethyl)-carbamoyl]-1,3-dioxo-5,8-dihydro-[1,2,4]triazolo[1,2-a]pyridazin-2-yl}-acrylic acid cyclohexyl ester(577793-31-8)

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: 577793-31-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 577793-31-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,7,7,9 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 577793-31:
(8*5)+(7*7)+(6*7)+(5*7)+(4*9)+(3*3)+(2*3)+(1*1)=218
218 % 10 = 8
So 577793-31-8 is a valid CAS Registry Number.

577793-31-8Upstream product

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577793-31-8Relevant academic research and scientific papers

High-throughput synthesis and optimization of thrombin inhibitors via urazole α-addition and Michael addition

Boatman, P. Douglas,Urban, Jan,Nguyen, Minh,Qabar, Maher,Kahn, Michael

, p. 1445 - 1449 (2003)

A novel α-addition of propiolates to urazoles followed by Michael addition of a variety of nucleophiles has been developed for rapid production and optimization of peptidomimetic drug leads. This technology has produced a number of highly potent and selective inhibitors of the serine protease, thrombin.

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