Cas 152297-24-0,(S)-2-[(E)-(S)-2-Methoxymethyl-pyrrolidin-1-ylimino]-1-methyl-cyclohexanecarbonitrile

152297-24-0

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Basic information

Product Name: (S)-2-[(E)-(S)-2-Methoxymethyl-pyrrolidin-1-ylimino]-1-methyl-cyclohexanecarbonitrile
Synonyms: (S)-2-[(E)-(S)-2-Methoxymethyl-pyrrolidin-1-ylimino]-1-methyl-cyclohexanecarbonitrile
CAS NO:152297-24-0
Molecular Formula:
Molecular Weight: 249.356
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: (S)-2-[(E)-(S)-2-Methoxymethyl-pyrrolidin-1-ylimino]-1-methyl-cyclohexanecarbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[(E)-(S)-2-Methoxymethyl-pyrrolidin-1-ylimino]-1-methyl-cyclohexanecarbonitrile(152297-24-0)
EPA Substance Registry System: (S)-2-[(E)-(S)-2-Methoxymethyl-pyrrolidin-1-ylimino]-1-methyl-cyclohexanecarbonitrile(152297-24-0)

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: 152297-24-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 152297-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,2,9 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 152297-24:
(8*1)+(7*5)+(6*2)+(5*2)+(4*9)+(3*7)+(2*2)+(1*4)=130
130 % 10 = 0
So 152297-24-0 is a valid CAS Registry Number.

152297-24-0Upstream product

152297-24-0Downstream Products

5670-51-9 (R)-1-methyl-2-oxocyclohexanecarbonitrile

152297-24-0Relevant academic research and scientific papers

Enantioselective synthesis of 2-alkyl-2-cyanocycloalkanones with a quaternary stereogenic center

Enders,Zamponi,Raabe,Runsink

, p. 725 - 728 (2007/10/02)

2-Alkyl-2-cyanocycloalkanones 4 bearing a quaternary stereogenic center are synthesized in good overall yields and high enantiomeric excesses (ee = 90-95%) employing the SAMP-/RAMP-hydrazone method. The absolute configuration is confirmed by NMR-spectroscopic investigations on SAMP-hydrazone 3a and an X-ray structure analysis of SAMP-hydrazone 3f.

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