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N,N-dimethyl-4-(propa-1,2-dien-1-yl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86448-32-0

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86448-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86448-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,4 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86448-32:
(7*8)+(6*6)+(5*4)+(4*4)+(3*8)+(2*3)+(1*2)=160
160 % 10 = 0
So 86448-32-0 is a valid CAS Registry Number.

86448-32-0Downstream Products

86448-32-0Relevant academic research and scientific papers

Synthesis of terminal allenes through copper-mediated cross-coupling of ethyne with N-tosylhydrazones or α-diazoesters

Ye, Fei,Wang, Chengpeng,Ma, Xiaoshen,Hossain, Mohammad Lokman,Xia, Ying,Zhang, Yan,Wang, Jianbo

, p. 647 - 652 (2016/09/12)

Ethyne is employed as coupling partner in coppermediated cross-coupling reactions with N-tosylhydrazones and α-diazoacetate, leading to the development of a new synthetic method for terminal allenes. With this novel coupling method, the terminal allenes w

Organomagnesium-catalyzed isomerization of terminal alkynes to allenes and internal alkynes

Rochat, Rapha?l,Yamamoto, Koji,Lopez, Michael J.,Nagae, Haruki,Tsurugi, Hayato,Mashima, Kazushi

supporting information, p. 8112 - 8120 (2015/05/27)

Organomagnesium complexes 2 were synthesized from N,N-dialkylamineimine ligands 1 and dibenzylmagnesium by benzylation of the imine moiety. 3-Aryl-1-propynes reacted with 2 to form the corresponding tetraalkynyl complexes, which acted as catalysts for the transformation of these terminal alkynes into allenes and further to internal alkynes under mild conditions. To the best of our knowledge, this example is the first of an organomagnesium-catalyzed isomerization of alkynes. Notably, the reactions proceeded through temporally separated autotandem catalysis, thus allowing the isolation of the allene or internal alkyne species in good yields. Mechanistic experiments suggested that the catalytically active tetraalkynyl complexes consist of a tautomeric mixture of alkynyl-, allenyl-, and propargylmagnesium species.

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