10541-69-2 | 2,5-Dichlorobenzylamine

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$31.00	$22.00
5g	97%	in stock	$57.00	$40.00
10g	97%	in stock	$92.00	$64.00
100g	97%	in stock	$760.00	$532.00

Description

• Catalog Number: AD45408
• Chemical Name: 2,5-Dichlorobenzylamine
• CAS Number: 10541-69-2
• Molecular Formula: C7H7Cl2N
• Molecular Weight: 176.0432
• MDL Number: MFCD00052391
• SMILES: NCc1cc(Cl)ccc1Cl

Computed Properties

• Complexity: 108
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2

Upstream Synthesis Route

(2,5-Dichlorophenyl)methanamine, also known as DCMA, is a versatile compound widely utilized in chemical synthesis. Its unique chemical structure with two chlorine atoms attached to a phenyl ring provides a range of reactivity ideal for various applications.In organic chemistry, (2,5-Dichlorophenyl)methanamine serves as a valuable building block for the synthesis of complex molecules. Its nucleophilic nature allows it to participate in a variety of reactions, including nucleophilic substitution, reductive amination, and cross-coupling reactions. These properties make DCMA a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals.Furthermore, (2,5-Dichlorophenyl)methanamine can be used in the development of novel materials and polymers. By incorporating DCMA into polymer chains, researchers can modify the material's properties, such as strength, flexibility, and thermal stability. This versatility makes DCMA a valuable tool for creating tailored materials for specific applications in industries like coatings, adhesives, and electronics.Overall, the application of (2,5-Dichlorophenyl)methanamine in chemical synthesis extends to various fields, showcasing its importance as a key building block for the development of diverse compounds and materials.

Literature

• OSCAR4: a flexible architecture for chemical text-mining.

  Journal of cheminformatics 20110101

• Synthesis of potential thrombin inhibitors. Incorporation of tartaric acid templates as P2 proline mimetics.

  Bioorganic & medicinal chemistry 20020501

• Benzylamines: synthesis and evaluation of antimycobacterial properties.

  Journal of medicinal chemistry 19840901