Cas 385435-05-2,(S)-N-(3-chlorophenylmethylidene)-1-[(1S,2R,4R)-7,7-dimethyl-2-(trimethylsilyloxy)bicyclo[2.2.1]heptan-1-yl]methanesulfinamide

385435-05-2

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Basic information

Product Name: (S)-N-(3-chlorophenylmethylidene)-1-[(1S,2R,4R)-7,7-dimethyl-2-(trimethylsilyloxy)bicyclo[2.2.1]heptan-1-yl]methanesulfinamide
Synonyms: (S)-N-(3-chlorophenylmethylidene)-1-[(1S,2R,4R)-7,7-dimethyl-2-(trimethylsilyloxy)bicyclo[2.2.1]heptan-1-yl]methanesulfinamide
CAS NO:385435-05-2
Molecular Formula:
Molecular Weight: 412.068
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)-N-(3-chlorophenylmethylidene)-1-[(1S,2R,4R)-7,7-dimethyl-2-(trimethylsilyloxy)bicyclo[2.2.1]heptan-1-yl]methanesulfinamide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-(3-chlorophenylmethylidene)-1-[(1S,2R,4R)-7,7-dimethyl-2-(trimethylsilyloxy)bicyclo[2.2.1]heptan-1-yl]methanesulfinamide(385435-05-2)
EPA Substance Registry System: (S)-N-(3-chlorophenylmethylidene)-1-[(1S,2R,4R)-7,7-dimethyl-2-(trimethylsilyloxy)bicyclo[2.2.1]heptan-1-yl]methanesulfinamide(385435-05-2)

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: 385435-05-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 385435-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,5,4,3 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 385435-05:
(8*3)+(7*8)+(6*5)+(5*4)+(4*3)+(3*5)+(2*0)+(1*5)=162
162 % 10 = 2
So 385435-05-2 is a valid CAS Registry Number.

385435-05-2Upstream product

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385435-05-2Relevant academic research and scientific papers

Addition of dienolates to sulfinimines. Stereoselective synthesis of dihydropyridones

Kaw, Robert

, p. 8385 - 8390 (2001)

The vinylogous Mannich reaction of sulfinimines with dienolates was investigated. Lithium and trimethylsilyl enolates of ethyl 3-ethoxycrotonate reacted with enantiopure 10-isobornylsulfinimines to give derivatives of δ-aminoacids which were cyclised to 6-aryl substituted derivatives of 2(1H)-pyridinones. 6-Aryl substituted 2,4-piperidinediones with either (S) or (R) configuration were analogously obtained using lithium and TMS enolates of 2,2,6-trimethyl-1,3-dioxin-4-one.

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