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CAS

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161622-27-1

10H-Quindoline-3,8-diamine, also known as 3,8-diaminoquindoline, is a heterocyclic aromatic compound belonging to the quinolines class with the molecular formula C9H9N3. It is a chemical compound that has garnered interest in the scientific community due to its potential applications in pharmaceuticals, including its use as a building block for synthesizing biologically active molecules, as well as its potential anticancer and antimicrobial properties.

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  • 161622-27-1 Structure

  • Basic information

    1. Product Name: 10H-QUINDOLINE-3,8-DIAMINE
    2. Synonyms: 10H-QUINDOLINE-3,8-DIAMINE
    3. CAS NO:161622-27-1
    4. Molecular Formula: C15H12N4
    5. Molecular Weight: 248.288
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 161622-27-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 625.3 °C at 760 mmHg
    3. Flash Point: 368.7 °C
    4. Appearance: /
    5. Density: 1.478 g/cm3
    6. Vapor Pressure: 1.49E-15mmHg at 25°C
    7. Refractive Index: 1.944
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 16.52±0.40(Predicted)
    11. CAS DataBase Reference: 10H-QUINDOLINE-3,8-DIAMINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 10H-QUINDOLINE-3,8-DIAMINE(161622-27-1)
    13. EPA Substance Registry System: 10H-QUINDOLINE-3,8-DIAMINE(161622-27-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 161622-27-1(Hazardous Substances Data)

161622-27-1 Usage

Uses

Used in Pharmaceutical Industry:
10H-Quindoline-3,8-diamine is used as a building block for the synthesis of various biologically active molecules, contributing to the development of new drugs with potential therapeutic applications.
Used in Anticancer Research:
10H-Quindoline-3,8-diamine is studied for its potential as an anticancer agent, with research focusing on its ability to inhibit the growth of cancer cells and its potential to be integrated into cancer treatment protocols.
Used in Antimicrobial Applications:
10H-Quindoline-3,8-diamine is also being investigated for its antimicrobial properties, which could lead to its use in the development of new antibiotics or antifungal agents to combat drug-resistant infections.
Used in Enzyme and Receptor Inhibition:
10H-Quindoline-3,8-diamine has been studied for its ability to inhibit certain enzymes and receptors in the body, making it a candidate for drug discovery and development, particularly for conditions that involve enzyme dysregulation or receptor overactivity.
Overall, 10H-Quindoline-3,8-diamine's multifaceted potential in various research areas positions it as a compound of interest for scientists exploring its therapeutic applications and furthering its development for clinical use.

Check Digit Verification of cas no

The CAS Registry Mumber 161622-27-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,6,2 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 161622-27:
(8*1)+(7*6)+(6*1)+(5*6)+(4*2)+(3*2)+(2*2)+(1*7)=111
111 % 10 = 1
So 161622-27-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H12N4/c16-9-2-1-8-5-14-15(19-12(8)6-9)11-4-3-10(17)7-13(11)18-14/h1-7,18H,16-17H2

161622-27-1SDS

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 10H-indolo[3,2-b]quinoline-3,8-diamine

1.2 Other means of identification

Product number -
Other names 10H-Quindoline-3,8-diamine

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:161622-27-1 SDS

161622-27-1Downstream Products

161622-27-1Relevant articles and documents

Structure Determination and Synthesis of Fluoro Nissl Green: An RNA-Binding Fluorochrome

Merlic, Craig A.,Motamed, Soheil,Quinn, Bruce

, p. 3365 - 3369 (2007/10/02)

The isolation, structure determination, and total synthesis of Fluoro Nissl Green, a novel RNA-binding fluorochrome, are reported.Initially obtained in only one part per 1E5, via a microwave-induced synthesis from m-phenylenediamine, the structure was det

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