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Benzenamine, N,N-dimethyl-4-(2-methyl-1-propenyl)-, also known as 4-isoprenyl-N,N-dimethylaniline or p-isoprenyl-N,N-dimethylaniline, is an organic compound with the chemical formula C12H19N. It is a derivative of aniline, featuring a dimethylamino group (-N(CH3)2) and a 2-methyl-1-propenyl (isoprenyl) group attached to the benzene ring. Benzenamine, N,N-dimethyl-4-(2-methyl-1-propenyl)- is characterized by its yellowish color and is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its potential applications in the production of polymers and as a precursor in the synthesis of natural products. Due to its reactivity, it is important to handle this chemical with care, following proper safety protocols.

4278-80-2

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4278-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4278-80-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4278-80:
(6*4)+(5*2)+(4*7)+(3*8)+(2*8)+(1*0)=102
102 % 10 = 2
So 4278-80-2 is a valid CAS Registry Number.

4278-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-4-(2-methylprop-1-enyl)aniline

1.2 Other means of identification

Product number -
Other names N.N-Dimethyl-4-(β.β-dimethyl-vinyl)-anilin

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:4278-80-2 SDS

4278-80-2Relevant academic research and scientific papers

Amido pincer nickel catalyzed kumada cross-coupling of aryl, heteroaryl, and vinyl chlorides

Zhang, Xue-Qi,Wang, Zhong-Xia

supporting information, p. 2081 - 2084 (2013/10/21)

Amido pincer nickel complexes {Ni(Cl)[2-P(Ph2)C 6H4NC(Ph)=NAr]} (Ar = 4-MeC6H4, 1; Ar = 4-ClC6H4, 2; Ar = 4-MeOC6H4, 3) were shown to efficiently catalyze the cross-coupling of activated, unactivated, and deactivated aryl chlorides, N-heteroaryl chlorides, 1,4-dichlorobenzene, and vinyl chlorides with aryl Grignard reagents. Georg Thieme Verlag Stuttgart, New York.

Development of a polymer bound Wittig reaction and use in multi-step organic synthesis for the overall conversion of alcohols to β-hydroxyamines

Bolli, Martin H.,Ley, Steven V.

, p. 2243 - 2246 (2007/10/03)

An efficient combinatorial access to β-hydroxyamines suitable for automation is achieved by the mild oxidation of alcohols to aldehydes by polymer supported perruthenate (PSP), the subsequent clean olefination of the obtained aldehydes by polymer supported Wittig reagents followed by the epoxidation of the olefins by dimethyldioxirane (DMDO), and the final aminolysis of the epoxides with various amines is described.

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