Cas 911694-30-9,((S)-1-Benzyloxymethyl-2-methyl-propyl)-[1-((R)-2-methyl-2H-pyridin-1-yl)-1-phenyl-meth-(E)-ylidene]-amine

911694-30-9

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Basic information

Product Name: ((S)-1-Benzyloxymethyl-2-methyl-propyl)-[1-((R)-2-methyl-2H-pyridin-1-yl)-1-phenyl-meth-(E)-ylidene]-amine
Synonyms: ((S)-1-Benzyloxymethyl-2-methyl-propyl)-[1-((R)-2-methyl-2H-pyridin-1-yl)-1-phenyl-meth-(E)-ylidene]-amine
CAS NO:911694-30-9
Molecular Formula:
Molecular Weight: 374.526
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)-1-Benzyloxymethyl-2-methyl-propyl)-[1-((R)-2-methyl-2H-pyridin-1-yl)-1-phenyl-meth-(E)-ylidene]-amine(CAS DataBase Reference)
NIST Chemistry Reference: ((S)-1-Benzyloxymethyl-2-methyl-propyl)-[1-((R)-2-methyl-2H-pyridin-1-yl)-1-phenyl-meth-(E)-ylidene]-amine(911694-30-9)
EPA Substance Registry System: ((S)-1-Benzyloxymethyl-2-methyl-propyl)-[1-((R)-2-methyl-2H-pyridin-1-yl)-1-phenyl-meth-(E)-ylidene]-amine(911694-30-9)

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: 911694-30-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 911694-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,6,9 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 911694-30:
(8*9)+(7*1)+(6*1)+(5*6)+(4*9)+(3*4)+(2*3)+(1*0)=169
169 % 10 = 9
So 911694-30-9 is a valid CAS Registry Number.

911694-30-9Upstream product

911694-30-9Downstream Products

911694-30-9Relevant academic research and scientific papers

New methodology toward chiral, non-racemic 2,5-cis-substituted piperidines via Suzuki cross-coupling

Larivee, Alexandre,Charette, Andre B.

, p. 3955 - 3957 (2007/10/03)

1,2,3,4-Tetrahydropyridines were halogenated upon treatment with iodine to obtain the desired cross-coupling precursors. Diastereoselective hydrogenation of Suzuki cross-coupling adducts allowed the facile asymmetric synthesis of 2,5-cis-substituted piper

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