Cas 865993-99-3,2-Methyl-propane-2-sulfinic acid [(R)-1-isopropyl-3-methyl-5-oxo-5-phenyl-pent-(Z)-ylidene]-amide

865993-99-3

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Basic information

Product Name: 2-Methyl-propane-2-sulfinic acid [(R)-1-isopropyl-3-methyl-5-oxo-5-phenyl-pent-(Z)-ylidene]-amide
Synonyms: 2-Methyl-propane-2-sulfinic acid [(R)-1-isopropyl-3-methyl-5-oxo-5-phenyl-pent-(Z)-ylidene]-amide
CAS NO:865993-99-3
Molecular Formula:
Molecular Weight: 335.511
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-Methyl-propane-2-sulfinic acid [(R)-1-isopropyl-3-methyl-5-oxo-5-phenyl-pent-(Z)-ylidene]-amide(CAS DataBase Reference)
NIST Chemistry Reference: 2-Methyl-propane-2-sulfinic acid [(R)-1-isopropyl-3-methyl-5-oxo-5-phenyl-pent-(Z)-ylidene]-amide(865993-99-3)
EPA Substance Registry System: 2-Methyl-propane-2-sulfinic acid [(R)-1-isopropyl-3-methyl-5-oxo-5-phenyl-pent-(Z)-ylidene]-amide(865993-99-3)

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: 865993-99-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 865993-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,9,9 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 865993-99:
(8*8)+(7*6)+(6*5)+(5*9)+(4*9)+(3*3)+(2*9)+(1*9)=253
253 % 10 = 3
So 865993-99-3 is a valid CAS Registry Number.

865993-99-3Upstream product

35660-91-4 (E)-1-phenyl-2-buten-1-one

865993-99-3Downstream Products

865993-99-3Relevant academic research and scientific papers

N-sulfinyl metalloenamine conjugate additions: Asymmetric synthesis of piperidines

Peltier, Hillary M.,Ellman, Jonathan A.

, p. 7342 - 7345 (2005)

The first examples of conjugate additions of W-tert-butanesulfmyl metalloenamines are reported. Highly stereoselective conjugate additions (97:3 to 99:1 dr) were observed between metalloenamines derived from N-sulfinyl ketimines and α,β-unsaturated ketone

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