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1,2,3-tribromo-6-methoxy-4-(4-methoxyphenyl)naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1414890-96-2

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1414890-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1414890-96-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,4,8,9 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1414890-96:
(9*1)+(8*4)+(7*1)+(6*4)+(5*8)+(4*9)+(3*0)+(2*9)+(1*6)=172
172 % 10 = 2
So 1414890-96-2 is a valid CAS Registry Number.

1414890-96-2Downstream Products

1414890-96-2Relevant academic research and scientific papers

Bromine-mediated cyclization of 1,4-diaryl buta-1,3-diyne to 1,2,3-tribromo-4-aryl naphthalene

Singha, Raju,Nandi, Sukla,Ray, Jayanta K.

, p. 6531 - 6534,4 (2012/12/11)

Bromine-mediated intramolecular cyclization of 1,4-diaryl buta-1,3-diynes has been developed for the construction of naphthalene motifs. A number of 1,2,3-tribromo-4-aryl naphthalenes are synthesized under mild reaction condition by the 6-endo-dig electro

Bromine-mediated cyclization of 1,4-diaryl buta-1,3-diyne to 1,2,3-tribromo-4-aryl naphthalene

Singha, Raju,Nandi, Sukla,Ray, Jayanta K.

, p. 6531 - 6534 (2013/01/15)

Bromine-mediated intramolecular cyclization of 1,4-diaryl buta-1,3-diynes has been developed for the construction of naphthalene motifs. A number of 1,2,3-tribromo-4-aryl naphthalenes are synthesized under mild reaction condition by the 6-endo-dig electro

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