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3934-20-1,MFCD00006061
Catalog No.:AA0032WI

3934-20-1 | 2,4-Dichloropyrimidine

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Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$6.00   $4.00
- +
10g
98%
in stock  
$7.00   $5.00
- +
25g
98%
in stock  
$16.00   $11.00
- +
100g
98%
in stock  
$53.00   $37.00
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500g
98%
in stock  
$83.00   $58.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0032WI
Chemical Name:
2,4-Dichloropyrimidine
CAS Number:
3934-20-1
Molecular Formula:
C4H2Cl2N2
Molecular Weight:
148.9781
MDL Number:
MFCD00006061
SMILES:
Clc1ccnc(n1)Cl
Properties
Properties
 
BP:
209.1°C at 760 mmHg  
Form:
Solid  
MP:
57-61 °C(lit.);  
Refractive Index:
1.6300 (estimate)  
Stability:
Moisture Sensitive  
Storage:
Keep in dry area;Room Temperature;  

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

Upstream Synthesis Route

[1]Patent:WO2010/20556,2010,A1,.Locationinpatent:Page/Pagecolumn62

[2]JournaloftheAmericanChemicalSociety,2003,vol.125,#33,p.9970-9982

[3]Tetrahedron,2010,vol.66,#6,p.1280-1288

[4]Patent:WO2006/114409,2006,A1,.Locationinpatent:Page/Pagecolumn18

[5]BioorganicandMedicinalChemistryLetters,1999,vol.9,#14,p.1973-1978

[6]ChemischeBerichte,1905,vol.38,p.1690

[7]ChemischeBerichte,1905,vol.38,p.1690

[8]JournaloftheAmericanChemicalSociety,1930,vol.52,p.1152,1156;vgl.H2480

[9]Heterocycles,2000,vol.53,#7,p.1489-1498

[10]Patent:US2007/238737,2007,A1,.Locationinpatent:Page/Pagecolumn11

[11]LettersinOrganicChemistry,2011,vol.8,#8,p.545-548

[12]ArchivderPharmazie,2014,vol.347,#2,p.77-88

[13]Patent:CN106317147,2017,A,.Locationinpatent:Paragraph0062;0063;0064;0065;0066;0067

[14]Patent:US2007/37974,2007,A1,.Locationinpatent:Page/Pagecolumn10

[1]JournaloftheAmericanChemicalSociety,1930,vol.52,p.1152,1156;vgl.H2480

[2]Patent:WO2008/70740,2008,A1,.Locationinpatent:Page/Pagecolumn201

[1]ChemischeBerichte,1905,vol.38,p.1690

[1]Patent:WO2009/42694,2009,A1,.Locationinpatent:Page/Pagecolumn83

[1]JournalofOrganicChemistry,2004,vol.69,#11,p.3943-3949

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1930,vol.52,p.1152,1156;vgl.H2480

[1]JournalofOrganicChemistry,2001,vol.66,p.7125-7128

[1]Bioorganicandmedicinalchemistryletters,2002,vol.12,p.3635-3639

[1]JournalofMedicinalChemistry,2004,vol.47,p.5057-5068

Literature

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

Journal: Chemical research in toxicology 20110718

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

Journal: Acta crystallographica. Section E, Structure reports online 20110601

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

Journal: Acta crystallographica. Section E, Structure reports online 20110601

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

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20110501

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

Journal: Bioorganic & medicinal chemistry letters 20110201

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

Journal: Chemistry Central journal 20110101

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

Journal: Chemical communications (Cambridge, England) 20100821

Title: 2,4-Dichloro-pyrimidine.

Journal: Acta crystallographica. Section E, Structure reports online 20090601

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

Journal: Nature chemical biology 20061101

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

Journal: Organic letters 20060119

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SDS
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