Cas 1123496-01-4,2-(3-(trifluoromethyl)phenyl)-1-(4-methoxypheny)-1-oxopropan-2-yl dimethyl phosphate

1123496-01-4

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Basic information

Product Name: 2-(3-(trifluoromethyl)phenyl)-1-(4-methoxypheny)-1-oxopropan-2-yl dimethyl phosphate
Synonyms: 2-(3-(trifluoromethyl)phenyl)-1-(4-methoxypheny)-1-oxopropan-2-yl dimethyl phosphate
CAS NO:1123496-01-4
Molecular Formula:
Molecular Weight: 432.333
EINECS: N/A
Product Categories: N/A
Mol File: 1123496-01-4.mol
Article Data: 1

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-(3-(trifluoromethyl)phenyl)-1-(4-methoxypheny)-1-oxopropan-2-yl dimethyl phosphate(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3-(trifluoromethyl)phenyl)-1-(4-methoxypheny)-1-oxopropan-2-yl dimethyl phosphate(1123496-01-4)
EPA Substance Registry System: 2-(3-(trifluoromethyl)phenyl)-1-(4-methoxypheny)-1-oxopropan-2-yl dimethyl phosphate(1123496-01-4)

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: 1123496-01-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1123496-01-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,3,4,9 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1123496-01:
(9*1)+(8*1)+(7*2)+(6*3)+(5*4)+(4*9)+(3*6)+(2*0)+(1*1)=124
124 % 10 = 4
So 1123496-01-4 is a valid CAS Registry Number.

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1123496-01-4Relevant articles and documents

Catalytic intermolecular Aldehyde-Ketone coupling via acyl phosphonates

Demir, Ayhan S.,Esiringue, Lker,Goellue, Mehmet,Reis, Oemer

supporting information; experimental part, p. 2197 - 2199 (2009/07/01)

The first catalytic intermolecular aldehyde-ketone coupling via acyl phosphonate is reported. Acyl phosphonates are potent acyl anion precursors, which generate acyl anion equivalents under the influence of cyanide anion via phosphonate-phosphate rearrang

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