Cas 352344-18-4,N-(p-methoxybenzyl)-4,9[1',2']benzeno-3a,4,9,9a-tetrahydro-1H-benz[f]isoindole-1,3(2H)-dione

352344-18-4

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Basic information

Product Name: N-(p-methoxybenzyl)-4,9[1',2']benzeno-3a,4,9,9a-tetrahydro-1H-benz[f]isoindole-1,3(2H)-dione
Synonyms: N-(p-methoxybenzyl)-4,9[1',2']benzeno-3a,4,9,9a-tetrahydro-1H-benz[f]isoindole-1,3(2H)-dione
CAS NO:352344-18-4
Molecular Formula:
Molecular Weight: 395.458
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: N-(p-methoxybenzyl)-4,9[1',2']benzeno-3a,4,9,9a-tetrahydro-1H-benz[f]isoindole-1,3(2H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: N-(p-methoxybenzyl)-4,9[1',2']benzeno-3a,4,9,9a-tetrahydro-1H-benz[f]isoindole-1,3(2H)-dione(352344-18-4)
EPA Substance Registry System: N-(p-methoxybenzyl)-4,9[1',2']benzeno-3a,4,9,9a-tetrahydro-1H-benz[f]isoindole-1,3(2H)-dione(352344-18-4)

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: 352344-18-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 352344-18-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,3,4 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 352344-18:
(8*3)+(7*5)+(6*2)+(5*3)+(4*4)+(3*4)+(2*1)+(1*8)=124
124 % 10 = 4
So 352344-18-4 is a valid CAS Registry Number.

352344-18-4Upstream product

352344-18-4Downstream Products

924626-20-0 N-(p-methoxybenzyl)-4,9[1',2']benzeno-1,3,3a,4,9,9a-hexahydro-1H-benz[f]isoindole

352344-18-4Relevant academic research and scientific papers

A novel design of roof-shaped anthracene-fused chiral prolines as organocatalysts for asymmetric Mannich reactions

Sasaoka, Aika,Uddin, Md. Imam,Shimomoto, Ai,Ichikawa, Yoshiyasu,Shiro, Motoo,Kotsuki, Hiyoshizo

, p. 2963 - 2969 (2006)

A new class of artificial anthracene-fused chiral proline catalysts has been synthesized from the Diels-Alder adduct of anthracene and maleic anhydride via lithiation/carboxylation of 6 as a key step. Chiral resolution of racemic amino acids was carried o

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