Cas 1361315-55-0,diisopropyl (2R,2'R)-2,2'-[diselane-1,2-diylbis(2,1-phenyleneoxy)]dipropanoate

1361315-55-0

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Basic information

Product Name: diisopropyl (2R,2'R)-2,2'-[diselane-1,2-diylbis(2,1-phenyleneoxy)]dipropanoate
Synonyms: diisopropyl (2R,2'R)-2,2'-[diselane-1,2-diylbis(2,1-phenyleneoxy)]dipropanoate
CAS NO:1361315-55-0
Molecular Formula:
Molecular Weight: 572.419
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: diisopropyl (2R,2'R)-2,2'-[diselane-1,2-diylbis(2,1-phenyleneoxy)]dipropanoate(CAS DataBase Reference)
NIST Chemistry Reference: diisopropyl (2R,2'R)-2,2'-[diselane-1,2-diylbis(2,1-phenyleneoxy)]dipropanoate(1361315-55-0)
EPA Substance Registry System: diisopropyl (2R,2'R)-2,2'-[diselane-1,2-diylbis(2,1-phenyleneoxy)]dipropanoate(1361315-55-0)

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: 1361315-55-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1361315-55-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,3,1 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1361315-55:
(9*1)+(8*3)+(7*6)+(6*1)+(5*3)+(4*1)+(3*5)+(2*5)+(1*5)=130
130 % 10 = 0
So 1361315-55-0 is a valid CAS Registry Number.

1361315-55-0Upstream product

1361315-55-0Downstream Products

1361315-59-4 isopropyl (2R)-2-(2-((2-methoxy-2-phenylethyl)selanyl)phenoxy)propanoate

1361315-55-0Relevant academic research and scientific papers

Asymmetric methoxyselenenylations with chiral selenium electrophiles

Zhao, Liwei,Li, Zhong,Wirth, Thomas

, p. 7080 - 7082 (2011)

Very simple, chiral, non-racemic diselenides were prepared and their corresponding selenium electrophiles were used for the stereoselective functionalization of alkenes. The influence of different alkenes on the outcome of the selenenylation reaction was

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