Cas 84942-83-6,hexakis[4-(ethoxycarbonyl)phenoxy]cyclotriphosphazene

84942-83-6

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Basic information

Product Name: hexakis[4-(ethoxycarbonyl)phenoxy]cyclotriphosphazene
Synonyms: hexakis[4-(ethoxycarbonyl)phenoxy]cyclotriphosphazene
CAS NO:84942-83-6
Molecular Formula:
Molecular Weight: 1125.95
EINECS: N/A
Product Categories: N/A
Mol File: 84942-83-6.mol
Article Data: 1

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: hexakis[4-(ethoxycarbonyl)phenoxy]cyclotriphosphazene(CAS DataBase Reference)
NIST Chemistry Reference: hexakis[4-(ethoxycarbonyl)phenoxy]cyclotriphosphazene(84942-83-6)
EPA Substance Registry System: hexakis[4-(ethoxycarbonyl)phenoxy]cyclotriphosphazene(84942-83-6)

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: 84942-83-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 84942-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,4 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84942-83:
(7*8)+(6*4)+(5*9)+(4*4)+(3*2)+(2*8)+(1*3)=166
166 % 10 = 6
So 84942-83-6 is a valid CAS Registry Number.

84942-83-6Upstream product

35285-68-8 sodium salt of ethyl-4-hydroxybenzoate

84942-83-6Downstream Products

84942-83-6Relevant articles and documents

Enantioselective adsorption of chiral amines on an induced helical poly(bis(4-carboxyphenoxy)phosphazene): Chiral filter effect

Maeda, Katsuhiro,Kuroyanagi, Kenji,Sakurai, Shin-Ichiro,Yamanaka, Toshio,Yashima, Eiji

, p. 2457 - 2464 (2011)

Optically inactive poly((bis(4-carboxyphenoxy)phosphazene) (poly-1) showed a large optical rotation upon complexation with optically active (R)- or (S)-1-phenylethylamine (2) in DMSO after annealing the complex solution at 65 °C for ca. 2 h and maintained

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