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2,4-Dichlorobenzaldehyde (benzothiazol-2-yl)hydrazone, commonly referred to as DBT hydrazone, is a versatile chemical compound characterized by its distinctive structure that includes a benzene ring with two chlorine atoms, a benzothiazole ring, and a hydrazone functional group. This unique molecular architecture endows it with specific reactivity and the capacity to form metal complexes, positioning it as a significant entity in the realms of organic synthesis and pharmaceutical research. Its potential as an anti-cancer agent, coupled with its applications in the development of new drugs and materials, renders DBT hydrazone a compelling subject for ongoing investigation and innovation.

73664-52-5

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73664-52-5 Usage

Uses

Used in Pharmaceutical Research and Development:
DBT hydrazone serves as a key intermediate in the synthesis of various pharmaceuticals, leveraging its ability to form metal complexes and its unique reactivity. It is particularly valuable in the development of novel drugs targeting cancer treatment.
Used in Organic Synthesis:
As a chemical compound with specific reactive sites, DBT hydrazone is utilized in organic synthesis to create a range of complex organic molecules, contributing to the advancement of material science and chemical technology.
Used in Cancer Treatment Research:
DBT hydrazone is explored as a potential anti-cancer agent, with ongoing studies aiming to understand its effects on different types of cancer cells. Its potential to interact with metal ions and form complexes that could have therapeutic effects makes it a promising candidate for cancer treatment.
Used in Material Science:
2,4-Dichlorobenzaldehyde (benzothiazol-2-yl)hydrazone's unique structure and reactivity also make it a candidate for the development of new materials with specific properties, such as those with applications in sensors, catalysts, or other high-tech industries.

Check Digit Verification of cas no

The CAS Registry Mumber 73664-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,6 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73664-52:
(7*7)+(6*3)+(5*6)+(4*6)+(3*4)+(2*5)+(1*2)=145
145 % 10 = 5
So 73664-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H9Cl2N3S/c15-10-6-5-9(11(16)7-10)8-17-19-14-18-12-3-1-2-4-13(12)20-14/h1-8H,(H,18,19)/b17-8+

73664-52-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(E)-(2,4-dichlorophenyl)methylideneamino]-1,3-benzothiazol-2-amine

1.2 Other means of identification

Product number -
Other names 2-[2-(2,4-dichlorobenzylidene)hydrazinyl]-1,3-benzothiazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:73664-52-5 SDS

73664-52-5Downstream Products

73664-52-5Relevant 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

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