Cas 145100-14-7,2H-Isoindole-1-carboxylic acid, 4,5,6,7-tetrahydro-3-[[5-oxo-1-(phenylmethyl)-2-pyrrolidinylidene]methyl] -, methyl ester, (Z)-

145100-14-7

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Basic information

Product Name: 2H-Isoindole-1-carboxylic acid, 4,5,6,7-tetrahydro-3-[[5-oxo-1-(phenylmethyl)-2-pyrrolidinylidene]methyl] -, methyl ester, (Z)-
Synonyms:
CAS NO:145100-14-7
Molecular Formula: C22H24N2O3
Molecular Weight: 364.444
EINECS: N/A
Product Categories: N/A
Mol File: 145100-14-7.mol

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: 2H-Isoindole-1-carboxylic acid, 4,5,6,7-tetrahydro-3-[[5-oxo-1-(phenylmethyl)-2-pyrrolidinylidene]methyl] -, methyl ester, (Z)-(CAS DataBase Reference)
NIST Chemistry Reference: 2H-Isoindole-1-carboxylic acid, 4,5,6,7-tetrahydro-3-[[5-oxo-1-(phenylmethyl)-2-pyrrolidinylidene]methyl] -, methyl ester, (Z)-(145100-14-7)
EPA Substance Registry System: 2H-Isoindole-1-carboxylic acid, 4,5,6,7-tetrahydro-3-[[5-oxo-1-(phenylmethyl)-2-pyrrolidinylidene]methyl] -, methyl ester, (Z)-(145100-14-7)

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: 145100-14-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 145100-14-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,1,0 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 145100-14:
(8*1)+(7*4)+(6*5)+(5*1)+(4*0)+(3*0)+(2*1)+(1*4)=77
77 % 10 = 7
So 145100-14-7 is a valid CAS Registry Number.

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145100-14-7Relevant academic research and scientific papers

Tetrapyrroles. IV. A highly efficient synthesis of homochiral dihydropyrromethenones via Pd○ mediated coupling of iodopyrroles and acetylenic amides

Jacobi, Peter A.,Rajeswari

, p. 6235 - 6238 (1992)

Homochiral dihydropyrromethenones of type 20 have been synthesized in a highly efficient manner by Pd○ mediated coupling of iodopyrrole 14 with acetylenic amides 18, followed by F- catalyzed 5-exo-dig cyclization. In analogous fashion, phytochr

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