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4-Bromobenzal of 2-Hydrazinobenzothiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32828-59-4

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32828-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32828-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,2 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32828-59:
(7*3)+(6*2)+(5*8)+(4*2)+(3*8)+(2*5)+(1*9)=124
124 % 10 = 4
So 32828-59-4 is a valid CAS Registry Number.

32828-59-4Relevant academic research and scientific papers

Synthesis and anticancer activity of (E)-2-benzothiazole hydrazones

Lindgren, Eric B.,De Brito, Monique A.,Vasconcelos, Thatyana R.A.,De Moraes, Manuel O.,Montenegro, Raquel C.,Yoneda, Julliane D.,Leal, Kátia Z.

, p. 12 - 16 (2014/09/29)

Benzothiazole hydrazones have been synthesized and evaluated for their in vitro antiproliferative activity against three human cancer cell lines: HL-60 (leukemia), MDAMB-435 (breast) and HCT-8 (colon). The good cytotoxicity for the three cancer cell lines

Synthesis and antitumor evaluation of (E)-2-benzothiazole hydrazones

Nogueira, Antonio Francisco,Azevedo, Elisa Carvalho,Ferreira, Vitor Francisco,Araujo, Ana Jersia,dos Santos, Evelyne Alves,Pessoa, Claudia,Costa-Lotufo, Leticia Veras,Montenegro, Raquel Carvalho,de Moraes, Manoel Odorico,Vasconcelos, Thatyana Rocha Alves

experimental part, p. 551 - 555 (2011/10/31)

A series of eleven (E)-2-benzothiazole hydrazones were synthesized and evaluated for their in vitro anticancer activities against three neoplastic cancer cells: HL-60 (leukemia), MDAMB-435 (breast) and HCT-8 (colon). Two of them, 3e and 3f, showed good cy

Preparation and Spectroscopic Properties of 2-Benzothiazolyl Araldehyde Hydrazones

Hearn, Michael J.,Schulz, Jeannette,Sinha, Anvita,Collins, Pamela,Hallenbeck, Susan,Kustin, Michael

, p. 521 - 524 (2007/10/02)

Notwithstanding its tendency toward air oxidation in solution, 2-hydrazinobenzothiazole I reacted with aromatic aldehydes in ethanol to give the corresponding hydrazones III-XV in high yields and analytical purity.In related examples, acylation took place

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