3934-20-1 | 2,4-Dichloropyrimidine

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$6.00	$4.00
10g	98%	in stock	$7.00	$5.00
25g	98%	in stock	$15.00	$11.00
100g	98%	in stock	$50.00	$35.00
500g	98%	in stock	$78.00	$55.00

Description

• Catalog Number: AB43630
• Chemical Name: 2,4-Dichloropyrimidine
• CAS Number: 3934-20-1
• Molecular Formula: C4H2Cl2N2
• Molecular Weight: 148.9781
• MDL Number: MFCD00006061
• SMILES: Clc1ccnc(n1)Cl

Computed Properties

• Complexity: 78.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 2.1

Literature

• Chemistry-based risk assessment for skin sensitization: quantitative mechanistic modeling for the S(N)Ar domain.

  Chemical research in toxicology 20110718

• 4,6-Dichloro-5-(2-meth-oxy-phen-oxy)-2,2'-bipyrimidine.

  Acta crystallographica. Section E, Structure reports online 20110601

• N-(2-Chloro-pyrimidin-4-yl)-2-methyl-2H-indazol-6-amine methanol monosolvate.

  Acta crystallographica. Section E, Structure reports online 20110601

• Molecular structure, harmonic and anharmonic frequency calculations of 2,4-dichloropyrimidine and 4,6-dichloropyrimidine by HF and density functional methods.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20110501

• Synthesis and antitumor activity of novel ribonucleosides with C-5 OH replaced by a diaminopyrimidinyl group.

  Bioorganic & medicinal chemistry letters 20110201

• Synthesis and characterization of novel 2, 2'-bipyrimidine fluorescent derivative for protein binding.

  Chemistry Central journal 20110101

• Unusual radical addition on a heteroaromatic nitrogen. A convenient access to new pyrimidine derivatives.

  Chemical communications (Cambridge, England) 20100821

• 2,4-Dichloro-pyrimidine.

  Acta crystallographica. Section E, Structure reports online 20090601

• Probing cell-division phenotype space and Polo-like kinase function using small molecules.

  Nature chemical biology 20061101

• An efficient route to 4-aryl-5-pyrimidinylimidazoles via sequential functionalization of 2,4-dichloropyrimidine.

  Organic letters 20060119