Cas 622840-45-3,(1R,2R,4R,S<sub>S</sub>)-N-[(1E)-benzylidene]-2-(2-trimethylsilyloxy-4-methylcyclohexyl)propane-2-sulfinamide

622840-45-3

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Basic information

Product Name: (1R,2R,4R,S_S)-N-[(1E)-benzylidene]-2-(2-trimethylsilyloxy-4-methylcyclohexyl)propane-2-sulfinamide
Synonyms: (1R,2R,4R,S_S)-N-[(1E)-benzylidene]-2-(2-trimethylsilyloxy-4-methylcyclohexyl)propane-2-sulfinamide
CAS NO:622840-45-3
Molecular Formula:
Molecular Weight: 379.639
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,4R,S_S)-N-[(1E)-benzylidene]-2-(2-trimethylsilyloxy-4-methylcyclohexyl)propane-2-sulfinamide(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,4R,S_S)-N-[(1E)-benzylidene]-2-(2-trimethylsilyloxy-4-methylcyclohexyl)propane-2-sulfinamide(622840-45-3)
EPA Substance Registry System: (1R,2R,4R,S_S)-N-[(1E)-benzylidene]-2-(2-trimethylsilyloxy-4-methylcyclohexyl)propane-2-sulfinamide(622840-45-3)

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: 622840-45-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 622840-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,2,8,4 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 622840-45:
(8*6)+(7*2)+(6*2)+(5*8)+(4*4)+(3*0)+(2*4)+(1*5)=143
143 % 10 = 3
So 622840-45-3 is a valid CAS Registry Number.

622840-45-3Upstream product

100-52-7 benzaldehyde

622840-45-3Downstream Products

622840-45-3Relevant academic research and scientific papers

New, recoverable and highly effective sulfinyl chiral auxiliary

Kawecki, Robert

, p. 2827 - 2832 (2003)

A facile synthesis of a bicyclic 8-menthylsulfinate is described. The reaction of this sultine with organometallic compounds leads to γ-hydroxysulfoxides, while the reaction with lithium amide affords 8-menthylsulfinamide. The chiral efficiency of the 8-m

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