Cas 188030-75-3,N,N'-(diselenodi-2,1-phenylenemethylene)bis[(2R,5R)-bis(methoxymethyl)pyrrolidine]

188030-75-3

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Basic information

Product Name: N,N'-(diselenodi-2,1-phenylenemethylene)bis[(2R,5R)-bis(methoxymethyl)pyrrolidine]
Synonyms: N,N'-(diselenodi-2,1-phenylenemethylene)bis[(2R,5R)-bis(methoxymethyl)pyrrolidine]
CAS NO:188030-75-3
Molecular Formula:
Molecular Weight: 654.61
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,N'-(diselenodi-2,1-phenylenemethylene)bis[(2R,5R)-bis(methoxymethyl)pyrrolidine](CAS DataBase Reference)
NIST Chemistry Reference: N,N'-(diselenodi-2,1-phenylenemethylene)bis[(2R,5R)-bis(methoxymethyl)pyrrolidine](188030-75-3)
EPA Substance Registry System: N,N'-(diselenodi-2,1-phenylenemethylene)bis[(2R,5R)-bis(methoxymethyl)pyrrolidine](188030-75-3)

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: 188030-75-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 188030-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,0,3 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 188030-75:
(8*1)+(7*8)+(6*8)+(5*0)+(4*3)+(3*0)+(2*7)+(1*5)=143
143 % 10 = 3
So 188030-75-3 is a valid CAS Registry Number.

188030-75-3Upstream product

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188030-75-3Relevant academic research and scientific papers

Design of optically active selenium reagents having a chiral tertiary amino group and their application to asymmetric inter- and intramolecular oxyselenenylations

Fujita, Ken-ichi,Murata, Kazuhisa,Iwaoka, Michio,Tomoda, Shuji

, p. 2029 - 2048 (2007/10/03)

A new class of chiral selenium reagents 4-7 was synthesized on the basis of the concept that the strong intramolecular interaction between an electrophilic selenium and an optically modified tertiary amine (Se··N interaction) would induce asymmetric induc

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