Cas 135128-18-6,2-(6,7-dihydro-6-methyl-5-oxo-5H-pyrrolo<3,4-b>pyridin-7-yl)-1,3-diphenyl-1,3-propanedione

135128-18-6

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Basic information

Product Name: 2-(6,7-dihydro-6-methyl-5-oxo-5H-pyrrolo<3,4-b>pyridin-7-yl)-1,3-diphenyl-1,3-propanedione
Synonyms: 2-(6,7-dihydro-6-methyl-5-oxo-5H-pyrrolo<3,4-b>pyridin-7-yl)-1,3-diphenyl-1,3-propanedione
CAS NO:135128-18-6
Molecular Formula:
Molecular Weight: 370.408
EINECS: N/A
Product Categories: N/A
Mol File: 135128-18-6.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: 2-(6,7-dihydro-6-methyl-5-oxo-5H-pyrrolo<3,4-b>pyridin-7-yl)-1,3-diphenyl-1,3-propanedione(CAS DataBase Reference)
NIST Chemistry Reference: 2-(6,7-dihydro-6-methyl-5-oxo-5H-pyrrolo<3,4-b>pyridin-7-yl)-1,3-diphenyl-1,3-propanedione(135128-18-6)
EPA Substance Registry System: 2-(6,7-dihydro-6-methyl-5-oxo-5H-pyrrolo<3,4-b>pyridin-7-yl)-1,3-diphenyl-1,3-propanedione(135128-18-6)

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: 135128-18-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135128-18-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,1,2 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135128-18:
(8*1)+(7*3)+(6*5)+(5*1)+(4*2)+(3*8)+(2*1)+(1*8)=106
106 % 10 = 6
So 135128-18-6 is a valid CAS Registry Number.

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135128-18-6Relevant articles and documents

Synthesis of 7-Substituted 6,7-Dihydro-5H-pyrrolopyridin-5-ones. Reaction of 7-Hydroxy Derivatives with Nucleophiles

Goto, Takehiko,Utsunomiya, Shin,Aiba, Hiroshi,Hayasaka, Hirotoka,Endo, Mikihiro,et al.

, p. 1901 - 1910 (2007/10/02)

Various 7-substituted 6,7-dihydro-5H-pyrrolopyridin-5-ones are synthesized by the reaction of the corresponding 7-hydroxy derivatives with nucleophiles involving active methylene compounds, aromatics, alcohols, p-toluenethiol, benzenesulfinic acid,

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