Cas 1094092-20-2,8-iodomethyl-2-phenyl-6-trifluoromethyl-4-oxa-1-azabicyclo[4.2.0]octan-5-one

1094092-20-2

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Basic information

Product Name: 8-iodomethyl-2-phenyl-6-trifluoromethyl-4-oxa-1-azabicyclo[4.2.0]octan-5-one
Synonyms:
CAS NO:1094092-20-2
Molecular Formula:
Molecular Weight: 411.162
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: 8-iodomethyl-2-phenyl-6-trifluoromethyl-4-oxa-1-azabicyclo[4.2.0]octan-5-one(CAS DataBase Reference)
NIST Chemistry Reference: 8-iodomethyl-2-phenyl-6-trifluoromethyl-4-oxa-1-azabicyclo[4.2.0]octan-5-one(1094092-20-2)
EPA Substance Registry System: 8-iodomethyl-2-phenyl-6-trifluoromethyl-4-oxa-1-azabicyclo[4.2.0]octan-5-one(1094092-20-2)

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: 1094092-20-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1094092-20-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,4,0,9 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1094092-20:
(9*1)+(8*0)+(7*9)+(6*4)+(5*0)+(4*9)+(3*2)+(2*2)+(1*0)=142
142 % 10 = 2
So 1094092-20-2 is a valid CAS Registry Number.

1094092-20-2Upstream product

1094092-20-2Downstream Products

1094092-20-2Relevant academic research and scientific papers

Iodocyclization of chiral cf3-allylmorpholinones: A versatile strategy for the synthesis of enantiopure α-Tfm-prolines and α-Tfm-dihydroxyprolines

Caupene, Caroline,Chaume, Gregory,Ricard, Louis,Brigaud, Thierry

body text, p. 209 - 212 (2009/06/20)

An efficient iodocyclization reaction of a chiral Tfm-allylmorpholinone provides a straightforward route to α-Tfm-prolines and α-Tfmdihydroxyprolines. The methodologies developed are particularly well adapted for gram-scale synthesis of enantiopure compou

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