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Benzenamine, 4-bromo-N-(phenylcarbonimidoyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53288-65-6

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53288-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53288-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,8 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53288-65:
(7*5)+(6*3)+(5*2)+(4*8)+(3*8)+(2*6)+(1*5)=136
136 % 10 = 6
So 53288-65-6 is a valid CAS Registry Number.

53288-65-6Relevant academic research and scientific papers

Tandem regioselective synthesis of tetrazoles and related heterocycles using iodine

Yella, Ramesh,Khatun, Nilufa,Rout, Saroj Kumar,Patel, Bhisma K.

, p. 3235 - 3245 (2011/06/20)

A one-pot, tandem process has been developed for the synthesis of a library of tetrazoles from aryl isothiocyanates. Condensation of aryl isothiocyanates with ammonia, and aryl amines (R-NH2) provided mono, 1,3-disubstituted symmetrical and unsymmetrical thioureas, which on desulfurization with molecular iodine (I2) led to formation of the corresponding heterocumulene (cyanamides or carbodiimides). The in situ generated heterocumulene on subsequent treatment with sodium azide at room temperature gave corresponding tetrazoles. The product regioselectivity for unsymmetrical 1,3-disubstituted thioureas was found to be correlated with the basicities (pKa's) of the parent amines attached to the thiourea. Aryl-sec-alkyl unsymmetrical thioureas gave thioamido guanidino products rather than the 5-aminotetrazoles produced by HgCl2 mediation of the reaction. Bis-thioureas derived from aryl isothiocyanates and hydrazine gave thiadiazoles exclusively.

A greener synthetic protocol for the preparation of carbodiimide

Ali, Abdur Rezzak,Ghosh, Harisadhan,Patel, Bhisma K.

experimental part, p. 1019 - 1021 (2010/04/02)

A new and facile preparation of symmetrical and unsymmetrical 1,3-diaryl and aryl-alkyl carbodiimides via a dehydrosulfurisation of their corresponding thioureas is described. Herein, the classical method of oxidative desulfurisation of thiourea to carbodiimide involving toxic heavy metal oxides (HgO) has been replaced with an easily available, cost-effective and environmentally benign reagent, iodine. Simple reaction conditions, easy purification of the products and high yields are important attributes of the present methodology and perhaps the best alternative from a green chemistry perspective. The only limitation to this method however, is in the preparation of 1,3-dialkyl substituted carbodiimide.

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