Cas 305330-86-3,Phosphonic acid, [2,2,2-trichloro-1-[(1-oxo-3-phenyl-2-propenyl)amino]ethyl]-, diethyl ester

305330-86-3

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Basic information

Product Name: Phosphonic acid, [2,2,2-trichloro-1-[(1-oxo-3-phenyl-2-propenyl)amino]ethyl]-, diethyl ester
Synonyms:
CAS NO:305330-86-3
Molecular Formula: C15H19Cl3NO4P
Molecular Weight: 414.653
EINECS: N/A
Product Categories: N/A
Mol File: 305330-86-3.mol

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, [2,2,2-trichloro-1-[(1-oxo-3-phenyl-2-propenyl)amino]ethyl]-, diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Phosphonic acid, [2,2,2-trichloro-1-[(1-oxo-3-phenyl-2-propenyl)amino]ethyl]-, diethyl ester(305330-86-3)
EPA Substance Registry System: Phosphonic acid, [2,2,2-trichloro-1-[(1-oxo-3-phenyl-2-propenyl)amino]ethyl]-, diethyl ester(305330-86-3)

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: 305330-86-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 305330-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,5,3,3 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 305330-86:
(8*3)+(7*0)+(6*5)+(5*3)+(4*3)+(3*0)+(2*8)+(1*6)=103
103 % 10 = 3
So 305330-86-3 is a valid CAS Registry Number.

305330-86-3Upstream product

305330-86-3Downstream Products

663177-35-3 diethyl 5-hydrazino-2-styryl-1,3-oxazol-4-ylphosphonate

305330-86-3Relevant academic research and scientific papers

A Facile Synthesis of Derivatives of (1,3,4-Thiadiazol-2-yl)glycine and Its Phosphonyl Analogue

Golovchenko, Aleksandr V.,Pilyo, Stepan G.,Brovarets, Vladimir S.,Chernega, Alexander N.,Drach, Boris S.

, p. 2851 - 2857 (2007/10/03)

The adducts formed by 4-functionally-substituted 2-aryl-5-hydrazino-1,3- oxazoles and aryl isothiocyanates recyclize on heating to produce the hitherto unknown derivatives of (1,3,4-thiadiazol-2-yl)glycine and its phosphonyl analogue.

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