Cas 732298-24-7,3-benzo[1,3]dioxol-5-ylmethyl-1-(2-<i>tert</i>-butyl-phenyl)-pyrrolidine-2,5-dione

732298-24-7

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Basic information

Product Name: 3-benzo[1,3]dioxol-5-ylmethyl-1-(2-tert-butyl-phenyl)-pyrrolidine-2,5-dione
Synonyms: 3-benzo[1,3]dioxol-5-ylmethyl-1-(2-tert-butyl-phenyl)-pyrrolidine-2,5-dione
CAS NO:732298-24-7
Molecular Formula:
Molecular Weight: 365.429
EINECS: N/A
Product Categories: N/A
Mol File: 732298-24-7.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: 3-benzo[1,3]dioxol-5-ylmethyl-1-(2-tert-butyl-phenyl)-pyrrolidine-2,5-dione(CAS DataBase Reference)
NIST Chemistry Reference: 3-benzo[1,3]dioxol-5-ylmethyl-1-(2-tert-butyl-phenyl)-pyrrolidine-2,5-dione(732298-24-7)
EPA Substance Registry System: 3-benzo[1,3]dioxol-5-ylmethyl-1-(2-tert-butyl-phenyl)-pyrrolidine-2,5-dione(732298-24-7)

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: 732298-24-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 732298-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,2,2,9 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 732298-24:
(8*7)+(7*3)+(6*2)+(5*2)+(4*9)+(3*8)+(2*2)+(1*4)=167
167 % 10 = 7
So 732298-24-7 is a valid CAS Registry Number.

732298-24-7Upstream product

732298-24-7Downstream Products

580-73-4 (+/-)-hinokinin

732298-24-7Relevant articles and documents

A novel asymmetric route to succinimides and derived compounds: Synthesis of the lignan lactone (+)-hinokinin

Bennett, D. Jonathan,Pickering, Paula L.,Simpkins, Nigel S.

, p. 1392 - 1393 (2007/10/03)

A novel approach to chiral succinimides and derived compounds has been developed that involves chiral lithium amide desymmetrisation of an N-ortho-tert-butylphenyl succinimide to generate a putative atropisomeric intermediate enolate, alkylation of which

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