Cas 134538-76-4,2,2'-di(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4'-di(tert-butyl)diphenylamine

134538-76-4

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Basic information

Product Name: 2,2'-di(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4'-di(tert-butyl)diphenylamine
Synonyms: 2,2'-di(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4'-di(tert-butyl)diphenylamine
CAS NO:134538-76-4
Molecular Formula:
Molecular Weight: 613.487
EINECS: N/A
Product Categories: N/A
Mol File: 134538-76-4.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: 2,2'-di(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4'-di(tert-butyl)diphenylamine(CAS DataBase Reference)
NIST Chemistry Reference: 2,2'-di(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4'-di(tert-butyl)diphenylamine(134538-76-4)
EPA Substance Registry System: 2,2'-di(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4'-di(tert-butyl)diphenylamine(134538-76-4)

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: 134538-76-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134538-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,5,3 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 134538-76:
(8*1)+(7*3)+(6*4)+(5*5)+(4*3)+(3*8)+(2*7)+(1*6)=134
134 % 10 = 4
So 134538-76-4 is a valid CAS Registry Number.

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134538-76-4Relevant articles and documents

REACTIONS OF DIARYLAMINES WITH HEXAFLUOROACETONE

Sviridov, V. D.,Chkanikov, N. D.,Kolomiets, A. F.,Fokin, A. V.

, p. 847 - 849 (2007/10/02)

Diphenylamine reacts with hexafluoroacetone to give a mixture of products, of which 2-(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)diphenylamine (II) was isolated.N-Arylanthranilic acids modify the 1,1,1,3,3,3-hexafluoro-2-hydroxy-2-propyl group upon the reaction of its sodium salt with the hydrate of hexafluoroacetone (I) under mild conditions.This method gave 4-(1-hydroxy-1-trifluoromethyl-2,2,3-trifluoroethyl)-N-(2,3-xylyl)anthranilic acid from N-(2,3-xylyl)anthranilic acid in 93percent yield.

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