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18300-67-9

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18300-67-9 Usage

General Description

4-(diethylamino)benzaldehyde thiosemicarbazone, also known as TABTS, is a chemical compound with the molecular formula C11H16N4S. It is a yellow solid that is a derivative of thiosemicarbazide and is used in various fields including pharmaceuticals, analytical chemistry, and biological research. TABTS has been studied for its potential as an anti-cancer agent due to its ability to inhibit the growth of cancer cells. It has also been used as a chelating agent for metal ions in analytical chemistry. Additionally, TABTS has shown potential as an anti-microbial agent, making it of interest for further research and development in the medical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 18300-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,0 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18300-67:
(7*1)+(6*8)+(5*3)+(4*0)+(3*0)+(2*6)+(1*7)=89
89 % 10 = 9
So 18300-67-9 is a valid CAS Registry Number.

18300-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [(E)-[4-(diethylamino)phenyl]methylideneamino]thiourea

1.2 Other means of identification

Product number -
Other names 4-Diaethylamino-benzaldehyd-thiosemicarbazon

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:18300-67-9 SDS

18300-67-9Relevant articles and documents

Effect of organic solvents on solvatochromic, fluorescence, and electrochemical properties of synthesized thiazolylcoumarin derivatives

Bahadur, Ali,Iqbal, Shahid,Ujan, Rabail,Channar, Pervaiz Ali,AL-Anazy, Murefah Mana,Saeed, Aamer,Mahmood, Qaiser,Shoaib, Muhammad,Shah, Mazloom,Arshad, Ifzan,Shabir, Ghulam,Saifullah, Muhammad,Liu, Guocong,Qayyum, Muhammad Abdul

, p. 1189 - 1197 (2021)

In this present investigation, thiazolylcoumarin derivatives (5a–5k) were synthesized from thiosemicarbazide, ethyl acetoacetate, and naphthaldehyde through a multistep route. The formation of thiazolylcoumarin derivatives with bioactive scaffolds was con

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