Cas 91376-68-0,Phosphonic acid, [1-(5-hexenylimino)-3-(4-nitrophenyl)-2-propenyl]-, diethyl ester

91376-68-0

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Basic information

Product Name: Phosphonic acid, [1-(5-hexenylimino)-3-(4-nitrophenyl)-2-propenyl]-, diethyl ester
Synonyms:
CAS NO:91376-68-0
Molecular Formula: C19H27N2O5P
Molecular Weight: 394.408
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: Phosphonic acid, [1-(5-hexenylimino)-3-(4-nitrophenyl)-2-propenyl]-, diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Phosphonic acid, [1-(5-hexenylimino)-3-(4-nitrophenyl)-2-propenyl]-, diethyl ester(91376-68-0)
EPA Substance Registry System: Phosphonic acid, [1-(5-hexenylimino)-3-(4-nitrophenyl)-2-propenyl]-, diethyl ester(91376-68-0)

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: 91376-68-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 91376-68-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,7 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91376-68:
(7*9)+(6*1)+(5*3)+(4*7)+(3*6)+(2*6)+(1*8)=150
150 % 10 = 0
So 91376-68-0 is a valid CAS Registry Number.

91376-68-0Upstream product

91376-68-0Downstream Products

91376-60-2 [2-(4-Nitro-phenyl)-1,6,7,8,9,9a-hexahydro-2H-quinolizin-4-yl]-phosphonic acid diethyl ester

91376-68-0Relevant academic research and scientific papers

PHOSPHORYL-SUBSTITUTED 1-AZADIENES FOR USE IN INTRAMOLECULAR DIELS-ALDER CYCLIZATIONS

Whitesell, Marilyn A.,Kyba, Evan P.

, p. 2119 - 2120 (1984)

The preparation and isolation of 2-(diethoxyphosphoryl)-1-azadienes and their use in the formation of functionalyzed quinolizidine and indolizidine ring systems via an intramolecular Diels-Alder reaction is described.

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