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83948-22-5

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83948-22-5 Usage

Chemical class

Pyrido[4,3-b]carbazole derivative

Explanation

The compound belongs to a class of chemical compounds derived from the pyrido[4,3-b]carbazole ring structure.

Explanation

The compound contains an ethylamino group (-NHCH2CH3) and a propylamino group (-NHCH2CH2CH3) attached to the pyrido[4,3-b]carbazole ring structure.

Explanation

The compound has a hydroxyl group (-OH) attached to the 9th position of the pyrido[4,3-b]carbazole ring.

Explanation

The compound has three methyl groups (-CH3) attached to the pyrido[4,3-b]carbazole ring at positions 5, 6, and 11.

Explanation

The molecular formula represents the total number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms in the compound.

Explanation

Due to its unique structure and properties, the compound may have various applications in these fields, such as in the development of new drugs, materials, or chemical processes.

Explanation

The solubility of the compound is not provided, but it may be influenced by the presence of polar and nonpolar functional groups in its structure.

Explanation

The stability of the compound is not provided, but it may be affected by various factors, including environmental conditions and the presence of other chemicals.

Explanation

The reactivity of the compound is not provided, but it may undergo reactions with other chemicals, such as acids, bases, or nucleophiles, depending on the presence of reactive functional groups.

Explanation

The compound has a complex structure with multiple functional groups and a large number of carbon atoms, making it a challenging target for synthesis and analysis.

Substituents

Ethylamino and propylamino groups

Hydroxyl group

Substituted at position 9

Methyl groups

Three methyl groups at positions 5, 6, and 11

Potential applications

Chemistry, pharmaceuticals, and materials science

Solubility

Unknown, but may vary depending on the solvent

Stability

Unknown, but may be influenced by factors such as temperature, pH, and exposure to light

Reactivity

Unknown, but may react with various reagents based on its functional groups

Structural complexity

High

Check Digit Verification of cas no

The CAS Registry Mumber 83948-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,4 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83948-22:
(7*8)+(6*3)+(5*9)+(4*4)+(3*8)+(2*2)+(1*2)=165
165 % 10 = 5
So 83948-22-5 is a valid CAS Registry Number.
InChI:InChI=1/C23H28N4O/c1-5-24-10-6-11-25-23-21-15(3)20-18-13-16(28)7-8-19(18)27(4)22(20)14(2)17(21)9-12-26-23/h7-9,12-13,24,28H,5-6,10-11H2,1-4H3,(H,25,26)

83948-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(ethylamino)propylamino]-5,6,11-trimethylpyrido[4,3-b]carbazol-9-ol

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:83948-22-5 SDS

83948-22-5Downstream Products

83948-22-5Relevant articles and documents

Antitumor Amino-Substituted Pyridopyrroloisoquinolines and Pyridocarbazole Derivatives: Synthesis and Evaluation of Compoudns Resulting from New Side Chain and Heterocycle Modifications

Rivalle, Christian,Wendling, Francoise,Tambourin, Pierre,Lhoste, Jean-Marc,Bisagni, Emile,Chermann, Jean-Claude

, p. 181 - 185 (2007/10/02)

New modifications of 10-amino>-6-methyl-5H-pyridopyrroloisoquinoline (1b) and 1-amino>-9-methoxy-5,11-dimethyl-6H-pyridocarbazole (4b), which display important antitumor properties

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