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63463-85-4

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63463-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63463-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,6 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63463-85:
(7*6)+(6*3)+(5*4)+(4*6)+(3*3)+(2*8)+(1*5)=134
134 % 10 = 4
So 63463-85-4 is a valid CAS Registry Number.

63463-85-4Downstream Products

63463-85-4Relevant academic research and scientific papers

Fast synthesis of hydrazine and Azo derivatives by oxidation of rare-earth-metal-nitrogen bonds

Zhang, Lijun,Xia, Jing,Li, Qinghai,Li, Xihong,Wang, Shaowu

, p. 375 - 378 (2011)

A novel N-N coupling reaction was developed through the oxidation of rare-earth-metal-nitrogen bonds produced by treatment of the easily available rare-earth-metal amides [(Me3Si)2N]3RE(μ-Cl) Li(THF)3 with aromatic primary or secondary amines. The reaction provides the symmetrical or unsymmetrical azo compounds and hydrazine derivatives in good to high yields within a very short time under mild conditions.

Photoisomerization of azobenzenes isolated in cryogenic matrices

Duarte, Luís,Khriachtchev, Leonid,Fausto, Rui,Reva, Igor

, p. 16802 - 16811 (2016/07/06)

2,2′-Dihydroxyazobenzene (DAB), 2,2′-azotoluene (AT) and azobenzene (AB) were isolated in argon and xenon matrices and their molecular structures and photochemical transformations were characterized by infrared spectroscopy and theoretical calculations. A

Sterically Hindered Azobenzenes: Isolation of Cis Isomers and Kinetics of Thermal Cis --> Trans Isomerization

Bunce, Nigel J.,Ferguson, George,Forber, Christine L.,Stachnyk, Greg J.

, p. 394 - 398 (2007/10/02)

A series of highly hindered ortho-alkylated azobenzenes has been isolated in the cis configuration for the first time.The crystal structure of one of these compounds, cis-2,2',6,6'-tetraisopropylazobenzene, shows that the molecule accommodates the bulky s

OXIDATION OF AROMATIC AMINES WITH CHROMYL CHLORIDE - I OXYDATION OF AROMATIC PRIMARY AMINES

Nallaiah, C.,Strickson, J. A.

, p. 4083 - 4088 (2007/10/02)

The oxidation of aromatic primary amines with chromyl chloride in carbon tetrachloride or chloroform, results in the formation of intermediate solid adducts (Etard adducts) which, on hydrolysis, give azobenzenes(1), 1,4-benzoquinones(2), anilino-1,4-benzoquinones(3), 1,4-benzoquinone anils(4) and anilino-1,4-benzoquinone anils(5) in yields which depend on the position, nature and degree of substitution of the ring.

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