Cas 1280199-34-9,(4R,6S)-6-hydroxy-4-phenyl-2-propyl-6-(trichloromethyl)-5,6-dihydro-4H-pyran-3-carbonitrile

1280199-34-9

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Basic information

Product Name: (4R,6S)-6-hydroxy-4-phenyl-2-propyl-6-(trichloromethyl)-5,6-dihydro-4H-pyran-3-carbonitrile
Synonyms: (4R,6S)-6-hydroxy-4-phenyl-2-propyl-6-(trichloromethyl)-5,6-dihydro-4H-pyran-3-carbonitrile
CAS NO:1280199-34-9
Molecular Formula:
Molecular Weight: 360.668
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: (4R,6S)-6-hydroxy-4-phenyl-2-propyl-6-(trichloromethyl)-5,6-dihydro-4H-pyran-3-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (4R,6S)-6-hydroxy-4-phenyl-2-propyl-6-(trichloromethyl)-5,6-dihydro-4H-pyran-3-carbonitrile(1280199-34-9)
EPA Substance Registry System: (4R,6S)-6-hydroxy-4-phenyl-2-propyl-6-(trichloromethyl)-5,6-dihydro-4H-pyran-3-carbonitrile(1280199-34-9)

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: 1280199-34-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1280199-34-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,0,1,9 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1280199-34:
(9*1)+(8*2)+(7*8)+(6*0)+(5*1)+(4*9)+(3*9)+(2*3)+(1*4)=159
159 % 10 = 9
So 1280199-34-9 is a valid CAS Registry Number.

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1280199-34-9Relevant academic research and scientific papers

Highly enantioselective synthesis of α-trichloromethyldihydropyrans catalyzed by bifunctional organocatalysts

Wang, Hai-Feng,Li, Peng,Cui, Hai-Feng,Wang, Xiao-Wei,Zhang, Jun-Kang,Liu, Wen,Zhao, Gang

supporting information; experimental part, p. 1774 - 1780 (2011/04/15)

The enantioselective Michael addition of α-cyanoketones to α,β-unsaturated trichloromethyl ketones was firstly reported. With a phenylalanine-derived bifunctional piperazine/thiourea catalyst, a series of α-trichloromethyldihydropyrans were obtained with

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