Cas 1032285-89-4,diethyl (1Z,3E)-5-(tert-butylamino)-5-oxo-2-phenylpenta-1,3-dienylphosphonate

1032285-89-4

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Basic information

Product Name: diethyl (1Z,3E)-5-(tert-butylamino)-5-oxo-2-phenylpenta-1,3-dienylphosphonate
Synonyms: diethyl (1Z,3E)-5-(tert-butylamino)-5-oxo-2-phenylpenta-1,3-dienylphosphonate
CAS NO:1032285-89-4
Molecular Formula:
Molecular Weight: 365.409
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: diethyl (1Z,3E)-5-(tert-butylamino)-5-oxo-2-phenylpenta-1,3-dienylphosphonate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl (1Z,3E)-5-(tert-butylamino)-5-oxo-2-phenylpenta-1,3-dienylphosphonate(1032285-89-4)
EPA Substance Registry System: diethyl (1Z,3E)-5-(tert-butylamino)-5-oxo-2-phenylpenta-1,3-dienylphosphonate(1032285-89-4)

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: 1032285-89-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1032285-89-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,2,8 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1032285-89:
(9*1)+(8*0)+(7*3)+(6*2)+(5*2)+(4*8)+(3*5)+(2*8)+(1*9)=124
124 % 10 = 4
So 1032285-89-4 is a valid CAS Registry Number.

1032285-89-4Upstream product

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1032285-89-4Relevant academic research and scientific papers

Palladium-catalyzed intermolecular ene-yne coupling: Development of an atom-efficient Mizoroki-Heck-type reaction

Lindhardt, Anders T.,Mantel, Mette Louise H.,Skrydstrup, Troels

, p. 2668 - 2672 (2008)

(Chemical Equation Presented) Direct and to the point: A palladium(II) catalytic system based on a palladium hydride species provides access to highly substituted 1,3-dienes through a direct coupling of alkynes with alkenes in a base-free Mizoroki-Heck-type reaction with full atom economy (see scheme; R=amide, borate, C(OH)Me2, O-alkyl).

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