2831-66-5 | 2,4-Dichloro-1,3,5-triazine

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$6.00	$4.00
1g	97%	in stock	$13.00	$9.00
5g	97%	in stock	$18.00	$13.00
10g	97%	in stock	$29.00	$20.00
25g	97%	in stock	$69.00	$49.00
100g	97%	in stock	$275.00	$192.00

Description

• Catalog Number: AB43616
• Chemical Name: 2,4-Dichloro-1,3,5-triazine
• CAS Number: 2831-66-5
• Molecular Formula: C3HCl2N3
• Molecular Weight: 149.9661
• MDL Number: MFCD04115347
• SMILES: Clc1ncnc(n1)Cl

Computed Properties

• Complexity: 70.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 3
• XLogP3: 1.9

Upstream Synthesis Route

2,4-Dichloro-1,3,5-triazine is a versatile chemical compound that finds wide application in various chemical synthesis processes. With its unique molecular structure and reactivity, 2,4-Dichloro-1,3,5-triazine serves as a valuable building block in the creation of pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, 2,4-Dichloro-1,3,5-triazine is commonly used as a reagent for the selective introduction of the triazine moiety into organic molecules. Its electrophilic nature allows it to react readily with nucleophiles, leading to the formation of novel compounds with diverse functionalities. The presence of two chlorine atoms on the triazine ring enhances its reactivity and enables precise control over the substitution patterns during synthesis.Furthermore, 2,4-Dichloro-1,3,5-triazine can undergo substitution reactions at both nitrogen and carbon atoms, offering flexibility in designing synthetic pathways for target molecules. Its compatibility with a range of functional groups makes it a valuable tool for the construction of complex chemical structures in a controlled manner.Overall, the use of 2,4-Dichloro-1,3,5-triazine in chemical synthesis allows researchers and chemists to access new synthetic routes, expand the chemical space of compounds, and accelerate the development of innovative materials with tailored properties.

Literature

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  Biomedical chromatography : BMC 20120601

• Application of cyanuric chloride-based six new chiral derivatizing reagents having amino acids and amino acid amides as chiral auxiliaries for enantioresolution of proteinogenic amino acids by reversed-phase high-performance liquid chromatography.

  Amino acids 20120401

• Application of amino acid amides as chiral auxiliaries in difluoro dinitro benzene and cyanuric chloride moieties for high-performance liquid-chromatographic enantioseparation of selenomethionine and its mixture with methionine and cysteine.

  Amino acids 20120401

• High-load, hybrid Si-ROMP reagents.

  Organic letters 20110107

• Targets in epigenetics: inhibiting the methyl writers of the histone code.

  Current chemical genomics 20110101

• Reversed-phase high-performance liquid chromatographic separation of diastereomers of (R,S)-mexiletine prepared by microwave irradiation with four new chiral derivatizing reagents based on trichloro-s-triazine having amino acids as chiral auxiliaries and 10 others having amino acid amides.

  Journal of chromatography. A 20101203

• Microwave-assisted synthesis and reversed-phase high-performance liquid chromatographic separation of diastereomers of (R,S)-baclofen using ten chiral derivatizing reagents designed from trichloro-s-triazine.

  Journal of chromatography. A 20101008

• Synthesis and characterization of a triazine dendrimer that sequesters iron(III) using 12 desferrioxamine B groups.

  Bioorganic & medicinal chemistry 20100801

• Design, synthesis, characterization, and biological evaluation of triazine dendrimers bearing paclitaxel using ester and ester/disulfide linkages.

  Bioconjugate chemistry 20091101

• Degradation of azo and anthraquinone dyes by a low-cost Fe 0/air process.

  Journal of hazardous materials 20090730

• High-load, oligomeric dichlorotriazine: a versatile ROMP-derived reagent and scavenger.

  The Journal of organic chemistry 20081121

• Triazine dendrimers with orthogonally protected amines on the periphery. Masking amines with Dde and BOC groups provides an alternative to carrying protected alcohols and disulfides through an iterative synthesis.

  The Journal of organic chemistry 20071221

• Formation and conformational conversion of flattened partial cone oxygen bridged calix[2]arene[2]triazines.

  Organic letters 20070719

• A divergent route to diversity in macromolecules.

  Organic letters 20060525

• New luminescent europium(III) chelates for DNA labeling.

  Inorganic chemistry 20060515

• Efficient labelling of antibodies with horseradish peroxidase using cyanuric chloride.

  Journal of immunological methods 20051130

• Magnetic dye affinity beads for the adsorption of beta-casein.

  Macromolecular bioscience 20050812

• Separation of lanthanides and actinides using magnetic silica particles bearing covalently attached tetra-CMPO-calix[4]arenes.

  Organic & biomolecular chemistry 20040821

• Heterogeneity of IgE epitopes of vinyl sulphone reactive dye: human serum albumin that react with IgE.

  Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 20011101

• Dye-ligand affinity systems.

  Journal of biochemical and biophysical methods 20011030

• Modulation of red blood cell aggregation and blood viscosity by the covalent attachment of Pluronic copolymers.

  Biorheology 20010101