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N-methyl-4-(1-phenylethyl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104903-68-6

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104903-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104903-68-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,0 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104903-68:
(8*1)+(7*0)+(6*4)+(5*9)+(4*0)+(3*3)+(2*6)+(1*8)=106
106 % 10 = 6
So 104903-68-6 is a valid CAS Registry Number.

104903-68-6Downstream Products

104903-68-6Relevant articles and documents

Catalytic alkylation of aromatic amines with styrene in the presence of cationic rhodium complexes and acid

Beller, Matthias,Thiel, Oliver R.,Trauthwein, Harald

, p. 243 - 245 (1999)

The first transition metal-catalyzed Friedel-Crafts alkylation of aromatic amines with styrene is reported. ortho-Alkylation of anilines occurs using catalytic amounts of [Rh(cod)2]BF4/4 PPh3 and HBF4.

REACTIONS OF STYRENE WITH AROMATIC AMINES

Olifirov, D. I.,Koshchii, V. A.,Kozlikovskii, Ya. B.

, p. 943 - 948 (2007/10/02)

In alkylation with styrene N,N-dimethylaniline in the presence of aluminum phenoxide, and aniline and N-methylaniline, also in the presence of aluminum phenoxide, as also of the corresponding hydrochlorides, usually form mixtures of mono(α-methylbenzyl)anilines, in which ortho-substitution products predominate.When aluminum phenoxide is used as catalyst, the yields of o-aralkylanilines attain 92-94percent.In the alkylation of N-methyl- and N,N-dimethyl-anilines demethylation and disproportionation occur.

MOLECULAR REARRANGEMENTS, XVIII. PHOTOLYSIS OF N-ALKYL-ARYLAMINES

Aly, Morsy M.,Badr, Mahmoud Zarif A.,Fahmy, Attiat M.,Mahgoub, Safaa A.

, p. 15 - 22 (2007/10/02)

The direct photolysis of N-benzyl-N-methyl-aniline in isopropanol at 25 deg C for 15 hours in air gives benzaldehyde, toluene, bibenzyl, N-methylaniline and a mixture of o- and p-benzyl-N-methylaniline.Analogous products are also obtained from the photolysis of N-α- or -β-phenethyl-N-methyl-aniline in addition to trans-2,3-diphenylbutene-2 and 9,10-dimethyl-phenanthrene.The results are interpreted in terms of an intramolecular free radical mechanism starting by homolysis of the N-aralkyl bond into N-methyl-anilino and aralkyl free radicals that subsequently contribute to the formation of the identified products.

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