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109322-11-4

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109322-11-4 Usage

Molecular structure

The compound has a complex molecular structure with multiple functional groups, including an indoloquinoxalinyl group, a phenylhydrazinecarbothioamide group, and an acetyl group.

Chlorine substitution

The presence of a 2-chloro substitution on the indoloquinoxalinyl group indicates the addition of a chlorine atom to the molecule, which can influence its chemical properties and reactivity.

Functional groups

The compound contains various functional groups, such as the indoloquinoxalinyl group, which is a fused ring system with electron-donating properties, and the phenylhydrazinecarbothioamide group, which is known for its biological activity and potential pharmaceutical applications.

Acetyl group

The presence of an acetyl group (-COCH3) in the compound suggests that it may have properties related to acetic acid, such as acidity or the ability to form hydrogen bonds.

Potential applications

The compound may have potential applications in various industries, including pharmaceuticals, agriculture, and materials science, due to its unique structure and functional groups. However, further research is needed to fully understand its properties and potential uses.

Stability and reactivity

The presence of multiple functional groups and a chlorine substitution may affect the compound's stability and reactivity, making it a subject of interest for further study.

Biological activity

The phenylhydrazinecarbothioamide group is known for its biological activity, which could indicate potential uses in pharmaceuticals or other biological applications.

Synthesis and purification

The complex structure of the compound may present challenges in its synthesis and purification, requiring specialized techniques and methods to obtain high-purity samples for study.

Physical and chemical properties

The compound's physical and chemical properties, such as solubility, melting point, and boiling point, may be influenced by its structure and functional groups, making it an interesting subject for further investigation.

Environmental and safety considerations

The presence of a chlorine atom in the compound may raise concerns about its environmental impact and safety, necessitating further research into its potential effects on ecosystems and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 109322-11-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,3,2 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 109322-11:
(8*1)+(7*0)+(6*9)+(5*3)+(4*2)+(3*2)+(2*1)+(1*1)=94
94 % 10 = 4
So 109322-11-4 is a valid CAS Registry Number.

109322-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[[2-(2-chloroindolo[2,3-b]quinoxalin-6-yl)acetyl]amino]-3-phenylthiourea

1.2 Other means of identification

Product number -
Other names -

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:109322-11-4 SDS

109322-11-4Relevant articles and documents

Synthesis of 2/9-Substituted Indophenazin-6-acetic Acid &α-Aryl/methylbenzylidenehydrazides, 4-Aryl-1-(indophenazin-6-methylcarbonyl)-3-thiosemicarbazides and 6-(4-Aryl-5-mercapto-4H-1,2,4-triazol-3-ylmethyl)indophenazines as CNS Active and Antiinflammato

Mohan, Rajiv Ravindra,Agarwal, Rajesh,Misra, V. S.

, p. 1234 - 1237 (2007/10/02)

2/9-Substituted indophenazine-6-acetic acid α-aryl/methylbenzylidenehydrazides (IVa-l) and 4-aryl-1-(2/9-substituted indophenazin-6-methylcarbonyl)-3-thiosemicarbazides (Va-j) have been synthesised by condensing 2/9-substituted indophenazin-6-acetic acid

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