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N,N-diallyl-N-(3-fluoro)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

188296-54-0

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188296-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188296-54-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,2,9 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 188296-54:
(8*1)+(7*8)+(6*8)+(5*2)+(4*9)+(3*6)+(2*5)+(1*4)=190
190 % 10 = 0
So 188296-54-0 is a valid CAS Registry Number.

188296-54-0Downstream Products

188296-54-0Relevant academic research and scientific papers

A general approach to substituted diphenyldiazenes

Lutz, Toni A.,Spanner, Patrick,Wanner, Klaus T.

, p. 1579 - 1589 (2016/03/01)

A general and practical synthetic method for the construction of unsymmetrically substituted diphenyldiazenes based on classical azo coupling reaction has been developed. A key feature of this method is the use of N,N-diallyl protected aniline derivatives

Highly selective N-allylation of anilines under microwave irradiation

Liu, Meiyu,Wang, Xie,Sun, Xiaoliang,He, Wei

, p. 2711 - 2714 (2014/05/06)

An easy and rapid procedure for the preparation of a variety of mono- and bis-allylated anilines via the reaction of allyl bromide with a wide range of anilines under microwave irradiation is described. This approach allows use of mild conditions and short reaction times to give high selectivities and excellent yields.

Assisted tandem catalytic RCM-aromatization in the synthesis of pyrroles and furans

Schmidt, Bernd,Krehl, Stefan,Jablowski, Eric

supporting information; experimental part, p. 5119 - 5130 (2012/08/07)

An assisted tandem catalytic transformation of diallyl amines and diallyl ethers into N-aryl pyrroles and furans, respectively, is described. The sequence relies on ring closing metathesis followed by dehydrogenation of the initially formed dihydropyrroles and dihydrofurans. Both steps are Ru-catalyzed, but the sequence requires only one precatalyst, because conversion of the metathesis catalyst into the dehydrogenation catalyst is achieved in situ, triggered by the oxidant tert-butyl hydroperoxide.

Synthesis of heterocyclic compounds by ring-closing metathesis (RCM): Preparation of oxygenated or nitrogenated compounds

Sanchez, Isabel,Pujol, Maria Dolors

, p. 1823 - 1828 (2007/10/03)

Novel methods for heterocyclic synthesis by metathesis have been developed. Versatile heterocyclic compounds were easily prepared in good yield from intermediate olefins by ring-closing olefin metathesis using the catalyst dichloro(benzylidene)bis(tricycl

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