Cas 150225-29-9,2-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl)-isoindole-1,3-dione

150225-29-9

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Basic information

Product Name: 2-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl)-isoindole-1,3-dione
Synonyms: 2-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl)-isoindole-1,3-dione
CAS NO:150225-29-9
Molecular Formula:
Molecular Weight: 607.267
EINECS: N/A
Product Categories: N/A
Mol File: 150225-29-9.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: 2-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl)-isoindole-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl)-isoindole-1,3-dione(150225-29-9)
EPA Substance Registry System: 2-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl)-isoindole-1,3-dione(150225-29-9)

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: 150225-29-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 150225-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,2,2 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 150225-29:
(8*1)+(7*5)+(6*0)+(5*2)+(4*2)+(3*5)+(2*2)+(1*9)=89
89 % 10 = 9
So 150225-29-9 is a valid CAS Registry Number.

150225-29-9Upstream product

85-44-9 phthalic anhydride

150225-29-9Downstream Products

139175-50-1 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecan-1-amine

150225-29-9Relevant articles and documents

Improved synthesis of perfluorooctylpropyl amine

Abulikemu, Abudurexiti,Halász, Gábor,Csámpai, Antal,G?m?ry, ágnes,Rábai, József

, p. 1143 - 1146 (2004)

Hydrazinolysis of N-perfluorooctylpropyl phthalimide is an easy route to scale up for the title compound. Both the alkylation of potassium phthalimide with perfluorooctylpropyl iodide and the hydrogenolysis of the adduct of perfluoroctyl iodide to N-allyl-phthalimide provide this amine precursor in good yields. The latter procedure, however, has a better atom economy, since it requires only three steps from perfluorooctyl iodide.

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