Cas 1032008-52-8,3-[4-(3-diisopropylamino-prop-1-ynyl)-phenyl]-1-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-propenone

1032008-52-8

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Basic information

Product Name: 3-[4-(3-diisopropylamino-prop-1-ynyl)-phenyl]-1-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-propenone
Synonyms: 3-[4-(3-diisopropylamino-prop-1-ynyl)-phenyl]-1-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-propenone
CAS NO:1032008-52-8
Molecular Formula:
Molecular Weight: 445.602
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: 3-[4-(3-diisopropylamino-prop-1-ynyl)-phenyl]-1-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-propenone(CAS DataBase Reference)
NIST Chemistry Reference: 3-[4-(3-diisopropylamino-prop-1-ynyl)-phenyl]-1-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-propenone(1032008-52-8)
EPA Substance Registry System: 3-[4-(3-diisopropylamino-prop-1-ynyl)-phenyl]-1-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-propenone(1032008-52-8)

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: 1032008-52-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1032008-52-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,0,0 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1032008-52:
(9*1)+(8*0)+(7*3)+(6*2)+(5*0)+(4*0)+(3*8)+(2*5)+(1*2)=78
78 % 10 = 8
So 1032008-52-8 is a valid CAS Registry Number.

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1032008-52-8Relevant academic research and scientific papers

Effect of varying the anionic component of a copper(I) catalyst on homologation of arylacetylenes to allenes by the Mannich reaction

Kumar, Vipan,Chipeleme, Alex,Chibale, Kelly

, p. 43 - 46 (2008/09/17)

The effect of varying the anionic component of a copper(I) catalyst in the homologation of terminal arylacetylenes to allenes by the Mannich reaction was investigated. Varying amounts of allenes, Mannich bases and dimers were obtained depending on the nature of the anionic component of the copper catalyst. On the other hand, Eglinton-Glaser dimerizations were achieved in high yields with 0.5 equiv. of triethylamine. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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