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2,3,6-tribromo-4-(p-tolylsulfonylamino)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107590-51-2

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107590-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107590-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,5,9 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107590-51:
(8*1)+(7*0)+(6*7)+(5*5)+(4*9)+(3*0)+(2*5)+(1*1)=122
122 % 10 = 2
So 107590-51-2 is a valid CAS Registry Number.

107590-51-2Relevant academic research and scientific papers

Synthesis of Polyhalogenated 2-Cyclohexane-1,4-dione Derivatives Containing Hydrogen at the sp3-Carbon Atoms from N-Arylsulfonyl-p-quinonimines and N,N'-Bis(arylsulfonyl)-p-quinonediimines

Avdeenko, A. P.,Zhukova, S. A.

, p. 388 - 396 (2007/10/03)

Chlorination and bromination of N-arylsulfonyl-1,4-benzo(naphtho)quinonimines, N,N'-bis(arylsulfonyl)-1,4-benzoquinonediimines, N-arylsulfonyl-4-aminophenols, and N-arylsulfonyl-4-aminonaphthols gave a number of stable polyhalogenated structures containing hydrogen at the sp3-hybridized carbon atoms. The chlorination and bromination schemes of N-arylsulfonyl-p-quinonimines are discussed.

BROMINATION OF 4-ARENESULFONAMIDOPHENOLS (OR 1-NAPHTHOLS) AND N-ARYLSULFONYL-1,4-BENZO(NAPHTHO)QUINON-4-IMINES

Avdeenko, A. P.,Velichko, N. V.

, p. 1687 - 1692 (2007/10/02)

2,3,6-Tribromo-N-phenylsulfonyl-1,4-benzoquinon-4-imines are formed on bromination of 4-arenesulfonamidophenols and N-aryl-sulfonyl-1,4-benzoquinon-4-imines but 2-bromo-N-arylsulfonyl-1,4-naphthoquinon-4-imines are formed from 4-arenesulfonamido-1-naphthols and N-arylsulfonyl-1,4-naphthoquinon-4-imines.

REACTION OF HYDROGEN BROMIDE WITH N-(p-TOLYL)- AND N-(p-TOLYLSULFONYL)-1,4-BENZOQUINONE MONOIMINES

Toropin, N. V.,Burmistrov, K. S.,Burmistrov, S. I.,Zaichenko, N. L.

, p. 894 - 899 (2007/10/02)

In the reaction of hydrogen bromide with N-(p-tolyl)-1,4-benzoquinone monoimines bromination of the p-tolyl fragment takes place as well as nucleophilic addition.Bromination is fully suppressed by the addition of resorcinol to the reaction mass.In the case of N-(p-tolylsulfonyl)-1,4-benzoquinone monoimine the products from the entry of two bromine atoms at the ortho position to the oxygen atom are formed sucessively.

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