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314084-63-4

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314084-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 314084-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,4,0,8 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 314084-63:
(8*3)+(7*1)+(6*4)+(5*0)+(4*8)+(3*4)+(2*6)+(1*3)=114
114 % 10 = 4
So 314084-63-4 is a valid CAS Registry Number.

314084-63-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-diethyl-4-phenylaniline

1.2 Other means of identification

Product number -
Other names 3,5-Diethyl-4-aminobiphenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:314084-63-4 SDS

314084-63-4Downstream Products

314084-63-4Relevant articles and documents

Room-temperature Suzuki-Miyaura cross-coupling reaction with α-diimine Pd(II) catalysts

Wang, Fuzhou,Tanaka, Ryo,Cai, Zhengguo,Nakayama, Yuushou,Shiono, Takeshi

, p. 771 - 776 (2015/11/09)

An α-diimine Pd(II) complex containing chiral sec-phenethyl groups, {bis[N,N′-(4-methyl-2-sec-phenethylphenyl)imino]-2,3-butadiene}dichloropalladium (rac-C1), was synthesized and characterized. rac-C1 was applied as an efficient catalyst for the Suzuki-Miyaura cross-coupling reaction between various aniline halides and arylboronic acid in PEG-400-H2O at room temperature. Among a series of aniline halides, rac-C1 did not catalyze the cross-coupling of aniline chlorides and fluorides but efficiently catalyzed the cross-coupling of aniline bromides and iodides with phenylboronic acid. The catalytic activity reduced slightly with increasing steric hindrance of the aniline bromides. The complexes {bis[N,N′-(4-fluoro-2,6-diphenylphenyl)imino]-2,3-butadiene}dichloropalladium and {bis[N,N′-(4-fluoro-2,6-diphenylphenyl)imino]acenaphthene}dichloropalladium were also found to be efficient catalysts for the reaction.

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