Cas 725724-49-2,(R)-2-Benzo[1,3]dioxol-5-ylmethyl-1,4-bis-((4S,5R)-3,4-dimethyl-2-oxo-5-phenyl-imidazolidin-1-yl)-butane-1,4-dione

725724-49-2

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Basic information

Product Name: (R)-2-Benzo[1,3]dioxol-5-ylmethyl-1,4-bis-((4S,5R)-3,4-dimethyl-2-oxo-5-phenyl-imidazolidin-1-yl)-butane-1,4-dione
Synonyms: (R)-2-Benzo[1,3]dioxol-5-ylmethyl-1,4-bis-((4S,5R)-3,4-dimethyl-2-oxo-5-phenyl-imidazolidin-1-yl)-butane-1,4-dione
CAS NO:725724-49-2
Molecular Formula:
Molecular Weight: 596.683
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: (R)-2-Benzo[1,3]dioxol-5-ylmethyl-1,4-bis-((4S,5R)-3,4-dimethyl-2-oxo-5-phenyl-imidazolidin-1-yl)-butane-1,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-Benzo[1,3]dioxol-5-ylmethyl-1,4-bis-((4S,5R)-3,4-dimethyl-2-oxo-5-phenyl-imidazolidin-1-yl)-butane-1,4-dione(725724-49-2)
EPA Substance Registry System: (R)-2-Benzo[1,3]dioxol-5-ylmethyl-1,4-bis-((4S,5R)-3,4-dimethyl-2-oxo-5-phenyl-imidazolidin-1-yl)-butane-1,4-dione(725724-49-2)

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: 725724-49-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 725724-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,5,7,2 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 725724-49:
(8*7)+(7*2)+(6*5)+(5*7)+(4*2)+(3*4)+(2*4)+(1*9)=172
172 % 10 = 2
So 725724-49-2 is a valid CAS Registry Number.

725724-49-2Upstream product

2606-51-1 3,4-Methylenedioxybenzyl bromide

725724-49-2Downstream Products

725724-49-2Relevant academic research and scientific papers

Highly diastereoselective alkylation of vicinal dianions of chiral succinic acid derivatives: A new general strategy to (R)-β-arylmethyl-γ- butyrolactones

Pohmakotr, Manat,Soorukram, Darunee,Tuchinda, Patoomratana,Prabpai, Samran,Kongsaeree, Palangpon,Reutrakul, Vichai

, p. 4315 - 4318 (2007/10/03)

The vicinal dianions derived from chiral succinic acid derivatives, 1,4-bis[(4R,5S)-3,4-dimethyl-2-oxo-5-phenylimidazolidin-1-yl]butane-1,4-dione and 1,4-bis[(4S,5R)-3,4-dimethyl-2-oxo-5-phenylimidazolidin-1-yl]butane-1,4- dione react with arylmethyl bromides with high diastereo- and regio-selectivity to provide the corresponding chiral α-arylmethylated succinic acid derivatives; the (R)-products are converted into (R)-β-arylmethyl-γ- butyrolactones and (R)-α-arylmethyl-γ-butyrolactones.

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