18528-78-4

• 

• Basic information

  1. Product Name: 2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE
  2. Synonyms: 3-Dihydro-1H-cyclopenta[b]quinolin-9-ylaMine;1H-Cyclopenta[b]quinolin-9-aMine, 2,3-dihydro-;1H,2H,3H-cyclopenta[b]quinolin-9-aMine;9-AMino-2,3-dihydro-1H-cyclopenta[b]quinoline;2,3-dihydro-9-amino-1h-cyclopenta(b)quinolin;2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE;2,3-Dihydro-1H-cyclopenta[b]quinolin-9-amine
  3. CAS NO:18528-78-4
  4. Molecular Formula: C12H12N2
  5. Molecular Weight: 184.24
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 18528-78-4.mol
  9. Article Data: 7

• Chemical Properties

  1. Melting Point: 175-176 °C
  2. Boiling Point: 394.5 °C at 760 mmHg
  3. Flash Point: 221 °C
  4. Appearance: /
  5. Density: 1.243 g/cm³
  6. Vapor Pressure: 1.97E-06mmHg at 25°C
  7. Refractive Index: 1.721
  8. Storage Temp.: 2-8°C(protect from light)
  9. Solubility: N/A
  10. PKA: 9.65±0.20(Predicted)
  11. CAS DataBase Reference: 2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE(CAS DataBase Reference)
  12. NIST Chemistry Reference: 2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE(18528-78-4)
  13. EPA Substance Registry System: 2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE(18528-78-4)

• 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: 18528-78-4(Hazardous Substances Data)

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• 2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-AMINE

  Cas No: 18528-78-4

• USD $ 3.0-3.0 / Kilogram

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• 2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE 18528-78-4

  Cas No: 18528-78-4

• USD $ 500.0-500.0 / Metric Ton

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• 2,3-Dihydro-1H-cyclopenta[b]quinolin-9-amine

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• 2,3-Dihydro-1H-cyclopenta[b]quinolin-9-ylamine

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• 2,3-Dihydro-1H-cyclopenta[b]quinolin-9-ylamine 18528-78-4 CAS NO.: 18528-78-4

  Cas No: 18528-78-4

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18528-78-4 Usage

General Description

2,3-Dihydro-1H-cyclopenta[b]quinolin-9-ylamine, also known as 9-amino-tetrahydroquinoline, is a chemical compound with potential pharmaceutical applications. It belongs to the class of organic compounds known as indolines, which are cyclic compounds containing an indole moiety, which consists of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. 2,3-DIHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE has been studied for its potential use as a building block in the synthesis of various biologically active molecules and pharmaceuticals. It is also being investigated for its potential pharmacological activities, such as its anti-inflammatory and anti-cancer properties. Further research is needed to fully understand and harness the potential of this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 18528-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,2 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18528-78:
(7*1)+(6*8)+(5*5)+(4*2)+(3*8)+(2*7)+(1*8)=134
134 % 10 = 4
So 18528-78-4 is a valid CAS Registry Number.

InChI:InChI=1/C12H12N2/c13-12-8-4-1-2-6-10(8)14-11-7-3-5-9(11)12/h1-2,4,6H,3,5,7H2,(H2,13,14)

18528-78-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	2,3-dihydro-1H-cyclopenta[b]quinolin-9-amine

1.2 Other means of identification

Product number	-
Other names	2,3-Dihydro-1H-cyclopenta[b]chinolin-9-ylamin

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:18528-78-4 SDS

18528-78-4Upstream product

• 40528-00-5 8-chloro-2,3-dihydro-1H-cyclopenta[1,2-b]quinoline 
• 97183-64-7 2-anilino-cyclopent-1-enecarbonitrile 
• 18528-77-3 9-bromo-2,3-dihydro-1H-cyclopenta[b]quinoline 
• 120-92-3 cyclopentanone 
• 1885-29-6 anthranilic acid nitrile 

18528-78-4Downstream Products

18528-78-4Related news

Design, synthesis, and biological evaluation of substituted 2,3-dihydro-1H-cyclopenta[b]quinolin-9-ylamine related compounds as fructose-1,6-bisphosphatase inhibitors09/05/2019

In a search for structurally new inhibitors of fructose-1,6-bisphosphatase (F16BPase), substituted 2,3-dihydro-1H-cyclopenta[b]quinoline derivatives were synthesized. It has been shown that the 2,3-dihydro-1H-cyclopenta[b]quinoline moiety may represent a suitable scaffold for the synthesis of po...detailed

18528-78-4Relevant articles and documents

Ionization constants of the drugs amiridin and tacrine and their analogs

Goncharenko,Kaganskii,Portnov,Granik

, p. 769 - 772 (1993)

-

A concise construction of polycyclic quinolines via annulation of ω-cyano-1-alkynes with diaryliodonium salts

Wang, Yong,Chen, Chao,Zhang, Shu,Lou, Zhenbang,Su, Xiang,Wen, Lirong,Li, Ming

supporting information, p. 4794 - 4797 (2013/10/08)

A concise construction of polycyclic quinolines via intramolecular [2 + 2 + 2] annulation of ω-cyano-1-alkynes with diaryliodonium salts was realized. The process produced polycyclic quinolines in high yields with readily available staring materials and was tolerated with halogen substituents.

Sulfuric acid-modified PEG-6000 (PEG-OSO3H): An efficient, bio-degradable and reusable polymeric catalyst for the solvent-free synthesis of poly-substituted quinolines under microwave irradiation

Hasaninejad, Alireza,Zare, Abdolkarim,Shekouhy, Mohsen,Ameri-Rad, Javad

experimental part, p. 958 - 964 (2011/05/12)

Sulfuric acid-modified polyethylene glycol 6000 (PEG-OSO3H) is applied as an efficient and eco-friendly polymeric catalyst for Friedlaender synthesis of poly-substituted quinolines from 2-aminoaryl ketones (or anthranilonitrile) and carbonyl compounds possessing a reactive methylene group under microwave irradiation and solvent-free conditions. The reactions are completed in short times, and the products are obtained in good to excellent yields. The Royal Society of Chemistry.

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