Cas 406225-93-2,(1R,2R)-N,N'-bis(5,5-dimethyl-2-oxo-2λ<sup>5</sup>-[1,3,2]dioxaphosphinan-2-yl)cyclohexane-1,2-diamine

406225-93-2

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Basic information

Product Name: (1R,2R)-N,N'-bis(5,5-dimethyl-2-oxo-2λ⁵-[1,3,2]dioxaphosphinan-2-yl)cyclohexane-1,2-diamine
Synonyms: (1R,2R)-N,N'-bis(5,5-dimethyl-2-oxo-2λ⁵-[1,3,2]dioxaphosphinan-2-yl)cyclohexane-1,2-diamine
CAS NO:406225-93-2
Molecular Formula:
Molecular Weight: 410.387
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: (1R,2R)-N,N'-bis(5,5-dimethyl-2-oxo-2λ⁵-[1,3,2]dioxaphosphinan-2-yl)cyclohexane-1,2-diamine(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R)-N,N'-bis(5,5-dimethyl-2-oxo-2λ⁵-[1,3,2]dioxaphosphinan-2-yl)cyclohexane-1,2-diamine(406225-93-2)
EPA Substance Registry System: (1R,2R)-N,N'-bis(5,5-dimethyl-2-oxo-2λ⁵-[1,3,2]dioxaphosphinan-2-yl)cyclohexane-1,2-diamine(406225-93-2)

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: 406225-93-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 406225-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,2,2 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 406225-93:
(8*4)+(7*0)+(6*6)+(5*2)+(4*2)+(3*5)+(2*9)+(1*3)=122
122 % 10 = 2
So 406225-93-2 is a valid CAS Registry Number.

406225-93-2Upstream product

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406225-93-2Relevant academic research and scientific papers

An approach to a chiral cycloalkanone-mediated asymmetric epoxidation of stilbene with oxone

Matsumoto,Tomioka

, p. 1653 - 1657 (2001)

Chiral and C2-symmetric seven-membered cycloalkanones 2 - 6 bearing 1,2-diphenylethane-1,2-diamine and cyclohexane-1,2-diamine backbones were synthesized and evaluated their asymmetry inductive behaviours in an asymmetric epoxidation of stilbene with oxon

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