Cas 130503-98-9,4-[4-(4-Methyl-thiazol-2-ylsulfanyl)-2,5-dioxo-1-phenyl-pyrrolidin-3-ylmethyl]-2-phenyl-tetrahydro-cyclopenta[c]pyrrole-1,3-dione

130503-98-9

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Basic information

Product Name: 4-[4-(4-Methyl-thiazol-2-ylsulfanyl)-2,5-dioxo-1-phenyl-pyrrolidin-3-ylmethyl]-2-phenyl-tetrahydro-cyclopenta[c]pyrrole-1,3-dione
Synonyms:
CAS NO:130503-98-9
Molecular Formula:
Molecular Weight: 531.656
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: 4-[4-(4-Methyl-thiazol-2-ylsulfanyl)-2,5-dioxo-1-phenyl-pyrrolidin-3-ylmethyl]-2-phenyl-tetrahydro-cyclopenta[c]pyrrole-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 4-[4-(4-Methyl-thiazol-2-ylsulfanyl)-2,5-dioxo-1-phenyl-pyrrolidin-3-ylmethyl]-2-phenyl-tetrahydro-cyclopenta[c]pyrrole-1,3-dione(130503-98-9)
EPA Substance Registry System: 4-[4-(4-Methyl-thiazol-2-ylsulfanyl)-2,5-dioxo-1-phenyl-pyrrolidin-3-ylmethyl]-2-phenyl-tetrahydro-cyclopenta[c]pyrrole-1,3-dione(130503-98-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 130503-98-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 130503-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,0 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 130503-98:
(8*1)+(7*3)+(6*0)+(5*5)+(4*0)+(3*3)+(2*9)+(1*8)=89
89 % 10 = 9
So 130503-98-9 is a valid CAS Registry Number.

130503-98-9Upstream product

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130503-98-9Relevant academic research and scientific papers

Cyclopentane ring formation in the cycloaddition reaction of 3-alkenyl radicals to radicophilic olefins

Saiic, Radomir N.,Cekovic, Zivorad

, p. 3627 - 3640 (1990)

Regioselective additions of 3-alkenyl radicals (10 and 20) to electron deficient olefinic bonds (7 and 17), followed by intramolecular 5- exo-cyclization and repeated addition to radicophilic double bonds were investigated and combined into a sequence of

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