Cas 1426097-64-4,2-((5S,6R,9S,10S)-3-cyclohexyl-7,9-dimethyl-4-oxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]dec-7-en-6-yl)acetaldehyde

1426097-64-4

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Basic information

Product Name: 2-((5S,6R,9S,10S)-3-cyclohexyl-7,9-dimethyl-4-oxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]dec-7-en-6-yl)acetaldehyde
Synonyms: 2-((5S,6R,9S,10S)-3-cyclohexyl-7,9-dimethyl-4-oxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]dec-7-en-6-yl)acetaldehyde
CAS NO:1426097-64-4
Molecular Formula:
Molecular Weight: 427.632
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: 2-((5S,6R,9S,10S)-3-cyclohexyl-7,9-dimethyl-4-oxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]dec-7-en-6-yl)acetaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 2-((5S,6R,9S,10S)-3-cyclohexyl-7,9-dimethyl-4-oxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]dec-7-en-6-yl)acetaldehyde(1426097-64-4)
EPA Substance Registry System: 2-((5S,6R,9S,10S)-3-cyclohexyl-7,9-dimethyl-4-oxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]dec-7-en-6-yl)acetaldehyde(1426097-64-4)

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: 1426097-64-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1426097-64-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,6,0,9 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1426097-64:
(9*1)+(8*4)+(7*2)+(6*6)+(5*0)+(4*9)+(3*7)+(2*6)+(1*4)=164
164 % 10 = 4
So 1426097-64-4 is a valid CAS Registry Number.

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1426097-64-4Relevant academic research and scientific papers

Aminocatalyzed asymmetric Diels-Alder reaction of 2,4-dienals and rhodanine/hydantoin derivatives

Zhu, Kailong,Huang, Huicai,Wu, Wenbin,Wei, Yuan,Ye, Jinxing

, p. 2157 - 2159 (2013)

Aminocatalyzed asymmetric Diels-Alder reaction between 2,4-dienals and rhodanine/hydantoin derivatives via trienamine mechanism has been developed to synthesize various spirocyclic compounds with good yields (up to 98%) and excellent stereoselectivities (

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