Cas 129368-96-3,[2-(1-Phenyl-ethylsulfanyl)-phenyl]-[(1R,4R)-1,7,7-trimethyl-bicyclo[2.2.1]hept-(2E)-ylidene]-amine

129368-96-3

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Basic information

Product Name: [2-(1-Phenyl-ethylsulfanyl)-phenyl]-[(1R,4R)-1,7,7-trimethyl-bicyclo[2.2.1]hept-(2E)-ylidene]-amine
Synonyms:
CAS NO:129368-96-3
Molecular Formula:
Molecular Weight: 363.567
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-(1-Phenyl-ethylsulfanyl)-phenyl]-[(1R,4R)-1,7,7-trimethyl-bicyclo[2.2.1]hept-(2E)-ylidene]-amine(CAS DataBase Reference)
NIST Chemistry Reference: [2-(1-Phenyl-ethylsulfanyl)-phenyl]-[(1R,4R)-1,7,7-trimethyl-bicyclo[2.2.1]hept-(2E)-ylidene]-amine(129368-96-3)
EPA Substance Registry System: [2-(1-Phenyl-ethylsulfanyl)-phenyl]-[(1R,4R)-1,7,7-trimethyl-bicyclo[2.2.1]hept-(2E)-ylidene]-amine(129368-96-3)

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: 129368-96-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129368-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,3,6 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129368-96:
(8*1)+(7*2)+(6*9)+(5*3)+(4*6)+(3*8)+(2*9)+(1*6)=163
163 % 10 = 3
So 129368-96-3 is a valid CAS Registry Number.

129368-96-3Upstream product

129368-96-3Downstream Products

129368-90-7 (2-Aminophenyl)-(1-phenylethyl)-sulfon

129368-96-3Relevant academic research and scientific papers

CHIRAL VARIANTS OF ARYLALKYL SULFUR REGENTS. (R)-CAMPHOR KETIMINES OF o-AMINOTHIOETHERS AND OXIDES

Delogu, Giovanna,de Lucchi, Ottorino,Fois, Maria Paola,Valle, Giovanni

, p. 417 - 425 (2007/10/02)

Ketimines 1a-d derived from ortho-aminosubstituted phenylthioethers wereprepared in order to determine the degree of chirality transfer from the auxiliary to the sulfur atom in the formation of the sulfoxide or to the α-carbon atom in the reaction of the

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