Welcome to LookChem.com Sign In|Join Free
  • or
2-Amino-5-chloroquinazoline is a chemical compound belonging to the quinazoline family, characterized by a molecular formula of C8H6ClN3. It is a solid, white to light yellow powder that exhibits sparing solubility in water but is more soluble in organic solvents. 2-Amino-5-chloroquinazoline is recognized for its potential applications in various fields, including pharmaceuticals, materials science, and as an antioxidant.

190273-70-2

Post Buying Request

190273-70-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

190273-70-2 Usage

Uses

Used in Pharmaceutical Industry:
2-Amino-5-chloroquinazoline is utilized as a building block for the synthesis of various biologically active compounds, playing a crucial role in the development of new drugs.
Used in Cancer Treatment:
In the field of oncology, 2-Amino-5-chloroquinazoline is studied for its potential therapeutic use against cancer, highlighting its capacity to contribute to the treatment of various types of malignancies.
Used in Antimicrobial Applications:
2-Amino-5-chloroquinazoline is employed as an antimicrobial agent, leveraging its properties to combat bacterial infections, making it a valuable component in the development of new antimicrobial drugs.
Used in Antifungal Applications:
Similarly, 2-Amino-5-chloroquinazoline is used as an antifungal agent, indicating its potential to be incorporated into treatments for fungal infections.
Used in Materials Science:
2-Amino-5-chloroquinazoline is also researched for its potential applications in materials science, where it may contribute to the creation of novel materials with specific properties.
Used as an Antioxidant:
Furthermore, 2-Amino-5-chloroquinazoline has been studied for its antioxidant properties, suggesting its use in applications requiring the prevention of oxidative damage, such as in the food industry or in cosmetic products.

Check Digit Verification of cas no

The CAS Registry Mumber 190273-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,2,7 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 190273-70:
(8*1)+(7*9)+(6*0)+(5*2)+(4*7)+(3*3)+(2*7)+(1*0)=132
132 % 10 = 2
So 190273-70-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClN3/c9-6-2-1-3-7-5(6)4-11-8(10)12-7/h1-4H,(H2,10,11,12)

190273-70-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Chloro-2-quinazolinamine

1.2 Other means of identification

Product number -
Other names 5-Chloroquinazolin-2-amine

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:190273-70-2 SDS

190273-70-2Downstream Products

190273-70-2Relevant academic research and scientific papers

NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS

-

Page/Page column 185, (2011/12/02)

Unsaturated nitrogen heterocyclic compounds of formula (I): (I), as defined in the specification, compositions containing them, and processes for preparing such compounds. Provided herein also are methods of treating disorders or diseases treatable by inhibition of PDE10, such as obesity, Huntington's Disease, non-insulin dependent diabetes, schizophrenia, bipolar disorder, obsessive-compulsive disorder, and the like.

Synthesis of 2-Aminoquinazolines from ortho-Fluorobenzaldehydes

Hynes, John B.,Campbell, Johnny P.

, p. 385 - 387 (2007/10/03)

The reaction of guanidine carbonate with various ortho-fluorobenzaldehydes in N,N-dimethylacetamide was investigated as a potential route for preparing 2-aminoquinazolines. Eleven new 2-aminoquinazolines were elaborated in this manner in low to moderate yields. In general the best results were obtained with ortho-fluorobenzaldehydes possessing an electron withdrawing substituent at the other ortho position. Complex mixtures were obtained using 2-fluorobenzaldehyde, 2,5-difluorobenzaldehyde and 2-fluoro-5-methoxybenzaldehyde which were not resolved.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 190273-70-2