Cas 93922-26-0,(3R,6S)-3-((R)-1-Methoxy-ethyl)-6-((S)-1-methoxy-ethyl)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile

93922-26-0

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Basic information

Product Name: (3R,6S)-3-((R)-1-Methoxy-ethyl)-6-((S)-1-methoxy-ethyl)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile
Synonyms:
CAS NO:93922-26-0
Molecular Formula:
Molecular Weight: 298.345
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: (3R,6S)-3-((R)-1-Methoxy-ethyl)-6-((S)-1-methoxy-ethyl)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (3R,6S)-3-((R)-1-Methoxy-ethyl)-6-((S)-1-methoxy-ethyl)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile(93922-26-0)
EPA Substance Registry System: (3R,6S)-3-((R)-1-Methoxy-ethyl)-6-((S)-1-methoxy-ethyl)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile(93922-26-0)

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: 93922-26-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 93922-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,2 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93922-26:
(7*9)+(6*3)+(5*9)+(4*2)+(3*2)+(2*2)+(1*6)=150
150 % 10 = 0
So 93922-26-0 is a valid CAS Registry Number.

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93922-26-0Relevant academic research and scientific papers

STEREOSELECTIVE SYNTHESIS AND DIELS-ALDER REACTIONS OF BIS-ETHER 1,3 DIENES. A FURTHER TEST FOR COOPERATIVITY DURING CYCLOADDITION REACTIONS.

Gree, Rene,Kessabi, Jilali,Mosset, Paul,Martelli, Jacques,Carrie, Robert

, p. 3697 - 3700 (2007/10/02)

A stereoselective synthesis of dienes 1a and 1b, using butadiene-iron tricarbonyl complexes, is described.Higher diastereoselectivity is observed during Diels-Alder reaction of 1a as compared with 1c, affording good evidence for cooperativity in these cycloadditions.

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