Cas 1335520-73-4,1-(1-(4-methoxyphenyl)-5-(4-(trifluoromethyl)phenyl)penta-1,4-diyn-3-yl)-2-methylbenzene

1335520-73-4

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Basic information

Product Name: 1-(1-(4-methoxyphenyl)-5-(4-(trifluoromethyl)phenyl)penta-1,4-diyn-3-yl)-2-methylbenzene
Synonyms: 1-(1-(4-methoxyphenyl)-5-(4-(trifluoromethyl)phenyl)penta-1,4-diyn-3-yl)-2-methylbenzene
CAS NO:1335520-73-4
Molecular Formula:
Molecular Weight: 404.431
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: 1-(1-(4-methoxyphenyl)-5-(4-(trifluoromethyl)phenyl)penta-1,4-diyn-3-yl)-2-methylbenzene(CAS DataBase Reference)
NIST Chemistry Reference: 1-(1-(4-methoxyphenyl)-5-(4-(trifluoromethyl)phenyl)penta-1,4-diyn-3-yl)-2-methylbenzene(1335520-73-4)
EPA Substance Registry System: 1-(1-(4-methoxyphenyl)-5-(4-(trifluoromethyl)phenyl)penta-1,4-diyn-3-yl)-2-methylbenzene(1335520-73-4)

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: 1335520-73-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1335520-73-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,5,5,2 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1335520-73:
(9*1)+(8*3)+(7*3)+(6*5)+(5*5)+(4*2)+(3*0)+(2*7)+(1*3)=134
134 % 10 = 4
So 1335520-73-4 is a valid CAS Registry Number.

1335520-73-4Upstream product

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1335520-73-4Relevant academic research and scientific papers

Aryl aldehydes as traceless dielectrophiles in bifunctional titanocene-catalyzed propargylic C-X activations

Campos, Catherine A.,Gianino, Joseph B.,Pinkerton, David M.,Ashfeld, Brandon L.

, p. 5680 - 5683 (2011)

The titanocene-catalyzed construction of all-carbon substituted tertiary centers directly from aromatic aldehydes is described. The starting aldehyde behaves as a traceless functionality in the formation of multiple carbon-carbon bonds through consecutive

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