Welcome to LookChem.com Sign In|Join Free

CAS

  • or

172604-85-2

Post Buying Request

172604-85-2 Suppliers

Recommended suppliersmore

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

172604-85-2 Usage

Chemical class

Quinolinone

Quinoline ring system

Present

Hydroxy group

At the 3 position

Methyl group

At the 1 position

2-Propenyl group

At the 4 position

Potential pharmaceutical activities

Anticancer, anti-inflammatory, and antifungal properties

Use in synthesis

Synthesis of other organic compounds

Potential applications

Development of new drugs and biologically active molecules

Therapeutic research

Research as a therapeutic agent in various medical conditions

Check Digit Verification of cas no

The CAS Registry Mumber 172604-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,6,0 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 172604-85:
(8*1)+(7*7)+(6*2)+(5*6)+(4*0)+(3*4)+(2*8)+(1*5)=132
132 % 10 = 2
So 172604-85-2 is a valid CAS Registry Number.

172604-85-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-allyl-3-hydroxy-1-methylquinolin-2(1H)-one

1.2 Other means of identification

Product number -
Other names 4-Allyl-3-hydroxy-1-methyl-1H-quinolin-2-one

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:172604-85-2 SDS

172604-85-2Downstream Products

172604-85-2Relevant articles and documents

Effect of substitution in stannic chloride-mediated heterocyclization of 4-allyl-3-hydroxyquinolin-2(1H)-ones

Majumdar,Kundu

, p. 3191 - 3201 (2006)

Effect of substituents at the allylic position in a stannic chloride-iodine-mediated heterocyclization of 4-allyl-3-hydroxyquinolin-2(1H)- ones for the regioselective formation of five- and six-membered heterocyclic rings has been rationalized by the application of restricted Hatree-Fock calculation. Copyright Taylor & Francis Group, LLC.

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

What can I do for you?
Get Best Price

Get Best Price for 172604-85-2