Cas 178933-30-7,Thioacetic acid S-{3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-1-[(S)-3-methyl-1-((S)-1-methylcarbamoyl-2-phenyl-ethylcarbamoyl)-butylcarbamoyl]-propyl} ester

178933-30-7

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Basic information

Product Name: Thioacetic acid S-{3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-1-[(S)-3-methyl-1-((S)-1-methylcarbamoyl-2-phenyl-ethylcarbamoyl)-butylcarbamoyl]-propyl} ester
Synonyms:
CAS NO:178933-30-7
Molecular Formula:
Molecular Weight: 580.705
EINECS: N/A
Product Categories: N/A
Mol File: 178933-30-7.mol
Article Data: 1

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: Thioacetic acid S-{3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-1-[(S)-3-methyl-1-((S)-1-methylcarbamoyl-2-phenyl-ethylcarbamoyl)-butylcarbamoyl]-propyl} ester(CAS DataBase Reference)
NIST Chemistry Reference: Thioacetic acid S-{3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-1-[(S)-3-methyl-1-((S)-1-methylcarbamoyl-2-phenyl-ethylcarbamoyl)-butylcarbamoyl]-propyl} ester(178933-30-7)
EPA Substance Registry System: Thioacetic acid S-{3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-1-[(S)-3-methyl-1-((S)-1-methylcarbamoyl-2-phenyl-ethylcarbamoyl)-butylcarbamoyl]-propyl} ester(178933-30-7)

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: 178933-30-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 178933-30-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,9,3 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 178933-30:
(8*1)+(7*7)+(6*8)+(5*9)+(4*3)+(3*3)+(2*3)+(1*0)=177
177 % 10 = 7
So 178933-30-7 is a valid CAS Registry Number.

178933-30-7Upstream product

178933-30-7Downstream Products

178933-30-7Relevant articles and documents

Mercaptoacyl matrix metalloproteinase inhibitors: The effect of substitution at the mercaptoacyl moiety

Baxter, Andrew D.,Bhogal, Ranjev,Bird, John B.,Buckley, George M.,Gregory, David S.,Hedger, Paul C.,Manallack, David T.,Massil, Tracy,Minton, Kevin J.,Montana, John G.,Neidle, Stephen,Owen, David A.,Watson, Robert J.

, p. 2765 - 2770 (2007/10/03)

The in vitro potency of orally-active mercaptoacyl matrix metalloproteinase inhibitors is increased by the introduction of appropriate substitutents on the mercaptoacyl moiety.

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