107-04-0 | 1-Bromo-2-chloroethane

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$26.00	$18.00
25g	98%	in stock	$40.00	$28.00
100g	98%	in stock	$90.00	$63.00
500g	98%	in stock	$307.00	$215.00

Description

• Catalog Number: AB50432
• Chemical Name: 1-Bromo-2-chloroethane
• CAS Number: 107-04-0
• Molecular Formula: C2H4BrCl
• Molecular Weight: 143.4102
• MDL Number: MFCD00000962
• SMILES: ClCCBr
• NSC Number: 60186

Computed Properties

• Complexity: 10
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 4
• Rotatable Bond Count: 1
• XLogP3: 1.6

Upstream Synthesis Route

1-Bromo-2-chloroethane, also known as ethylene chlorobromide, is a versatile compound commonly used in chemical synthesis. This compound serves as a valuable building block for the production of a wide range of chemicals, including pharmaceuticals, pesticides, and specialty materials. In chemical synthesis, 1-Bromo-2-chloroethane is often employed as a reagent for various reactions due to its unique properties and reactivity. It can undergo substitution reactions, addition reactions, and elimination reactions, making it a versatile intermediate in organic synthesis. Additionally, the presence of both bromine and chlorine atoms in the molecule imparts specific chemical properties that enable the selective functionalization of different positions in more complex molecules. Due to its flexibility and utility in various synthetic pathways, 1-Bromo-2-chloroethane plays a crucial role in the creation of a wide array of chemical compounds with diverse applications in industry and research.

Literature

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  The Journal of organic chemistry 20111202

• Dissociative double ionization of 1-bromo-2-chloroethane irradiated by an intense femtosecond laser field.

  The Journal of chemical physics 20110814

• Coherent control of the ultrafast dissociative ionization dynamics of bromochloroalkanes.

  Physical chemistry chemical physics : PCCP 20110521

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  Acta crystallographica. Section E, Structure reports online 20110201

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  Nature chemical biology 20091001

• Discovery of leukotriene A4 hydrolase inhibitors using metabolomics biased fragment crystallography.

  Journal of medicinal chemistry 20090813

• A conformational study of 1-bromo-2-chloroethane in zeolites.

  Langmuir : the ACS journal of surfaces and colloids 20090721

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  Physical review letters 20060505

• Efficient synthesis of furan-2-ylacetates, 7-(alkoxycarbonyl)benzofurans, and 7-(alkoxycarbonyl)-2,3-dihydrobenzofurans based on cyclization reactions of free and masked dianions: a 'cyclization/dehydrogenation' strategy.

  The Journal of organic chemistry 20051125

• Obtaining the structure and bond rotational potential of a substituted ethane by NMR spectroscopy of solutions in nematic liquid-crystalline solvents.

  The Journal of chemical physics 20051115

• Synthesis and biological activity of 1H-benzotriazole and 1H-benzimidazole analogues--inhibitors of the NTpase/helicase of HCV and of some related Flaviviridae.

  Antiviral chemistry & chemotherapy 20050101

• Chemoselective, regioselective, and E/Z-diastereoselective synthesis of 2-alkylidenetetrahydrofurans by sequential reactions of ambident dianions and monoanions.

  The Journal of organic chemistry 20031212