Welcome to LookChem.com Sign In|Join Free
  • or
1,3,8-trimethylpyrimido[4,5-b]quinoline-2,4(1H,3H)-dione is a complex organic compound with the molecular formula C16H14N2O2. It is characterized by a pyrimido[4,5-b]quinoline core structure, which features a fused pyrimidine and quinoline ring system. The compound is further defined by the presence of three methyl groups attached to the 1st, 3rd, and 8th carbon atoms of the molecule. The numbering of the carbon atoms is based on the standard nomenclature for such structures. The compound also has two carbonyl groups (dione), one at the 2nd position and the other at the 4th position, which are part of the 1H and 3H tautomeric forms, indicating the presence of hydrogen atoms that can shift between these positions, affecting the compound's reactivity and properties. 1,3,8-trimethylpyrimido[4,5-b]quinoline-2,4(1H,3H)-dione is likely to be of interest in the field of organic chemistry, potentially for its pharmacological or chemical properties, although specific applications or uses are not detailed in this summary.

73029-28-4

Post Buying Request

73029-28-4 Suppliers

Recommended suppliers

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

73029-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73029-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,2 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73029-28:
(7*7)+(6*3)+(5*0)+(4*2)+(3*9)+(2*2)+(1*8)=114
114 % 10 = 4
So 73029-28-4 is a valid CAS Registry Number.

73029-28-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,8-trimethylpyrimido[4,5-b]quinoline-2,4-dione

1.2 Other means of identification

Product number -
Other names 1,3,8-trimethyl-1,2,3,4-tetrahydropyrimido[4,5-b]quinoline-2,4-dione

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:73029-28-4 SDS

73029-28-4Downstream Products

73029-28-4Relevant academic research and scientific papers

Synthesis of pyrimidine fused quinolines by ligand-free copper-catalyzed domino reactions

Panday, Anoop Kumar,Mishra, Richa,Jana, Asim,Parvin, Tasneem,Choudhury, Lokman H.

, p. 3624 - 3632 (2018/04/14)

Herein, we report two novel methods for the synthesis of pyrimidine fused quinolines using a one-pot C-C and C-N bond forming strategy from the reaction of 6-aminouracils with 2-bromobenzaldehydes or 2-bromobenzyl bromide derivatives in the presence of 10 mol % CuCl2 without using any ligand. The reaction of 2-bromobenzaldehyde or its derivatives with 6-aminouracils in the presence of K2CO3 as base and a catalytic amount of CuCl2 in DMF medium under microwave heating conditions provides corresponding pyrimidine fused quinoline derivatives in good yields within 30 min. Alternatively, pyrimidine fused quinoline derivatives have been synthesized from the reaction of 2-bromobenzyl bromides with 6-aminouracil derivatives in the presence of molecular oxygen, CuCl2 (10 mol %), and K2CO3 as base in DMF under reflux conditions. Structures of all the products were unambiguously confirmed by spectroscopic techniques and by recording single crystal XRD of 3a.

Spectroscopy and photophysics of trimethyl-substituted derivatives of 5-deazaalloxazine. Experimental and theoretical approaches

Pruka?a, Dorota,Gierszewski, Mateusz,Kubicki, Maciej,P?dziński, Tomasz,Sikorska, Ewa,Sikorski, Marek

, p. 139 - 146 (2015/02/19)

Photophysical and structural properties of 5-deazaalloxazine derivatives were studied, with methyl substituent at the position 8 or 9 of the benzene ring and at the N(1) and N(3) positions. Crystal structures of the compounds were determined by X-ray diff

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 73029-28-4