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Halides / Halide containing compounds


Organic halides are a large group of chemicals that contain at least one halogen atom, also known as halogenated compounds or organohalogens. They can be prepared by different type of halogenations (radical, electrophilic addition, α-keto halogenation) which depends on nature of substrate. The facility of halogenation is influenced by the halogen. Fluorine and chlorine are more electrophilic and are more aggressive halogenating agents while bromine is a weaker and iodine is the least reactive of them all. The facility of reactivity follows the reverse trend: iodine is most easily removed from organic compounds and organofluorine compounds are highly stable. Many organohalogens are important synthetic intermediates, suitable for further transformations like substitutions or couplings. They are often used in industry as solvents, pesticides, refrigerants, fire-resistant oils, ingredients of elastomers, adhesives and sealants, electrically insulating coatings, plasticizers, and plastics.

Product nameStructureCAS#G-code
6-Bromo-2,4,5-trichlorophenolStructure of 6-Bromo-2,4,5-trichlorophenol[4524-78-1]GEO-00592
4-Bromo-2-(trifluoromethyl)phenyl isocyanateStructure of 4-Bromo-2-(trifluoromethyl)phenyl isocyanate[186589-12-8]GEO-02901
2-Bromo-5-trifluoromethylthiopheneStructure of 2-Bromo-5-trifluoromethylthiophene[143469-22-1]GEO-03957
11-Bromo-1-undeceneStructure of 11-Bromo-1-undecene[7766-50-9]GEO-03714
5-BromouridineStructure of 5-Bromouridine[957-75-5]GEO-00597
p-tert-Butylbenzyl bromideStructure of p-tert-Butylbenzyl bromide[18880-00-7]GEO-00611
tert-Butyl 3-(4-fluorophenyl)-4-oxopiperidine-1-carboxylateStructure of tert-Butyl 3-(4-fluorophenyl)-4-oxopiperidine-1-carboxylate[632352-74-0]GEO-04180
tert-ButylhypochloriteStructure of tert-Butylhypochlorite[507-40-4]GEO-03098
NewCapecitabineStructure of Capecitabine[154361-50-9]GEO-04908
Chloroacetyl isocyanateStructure of Chloroacetyl isocyanate[4461-30-7]GEO-02756
6-Chloro-m-anisidineStructure of 6-Chloro-m-anisidine[2401-24-3]GEO-02472
6-Chloro-m-anisidine hydrochlorideStructure of 6-Chloro-m-anisidine hydrochloride[85006-21-9]GEO-00648
4-Chlorobenzenesulfonyl isocyanateStructure of 4-Chlorobenzenesulfonyl isocyanate[5769-15-3]GEO-00652
2-Chloro-1H-benzimidazoleStructure of 2-Chloro-1H-benzimidazole[4857-06-1]GEO-00651
2-ChlorobenzothiazoleStructure of 2-Chlorobenzothiazole[615-20-3]GEO-00655
3-Chlorobenzo[b]thiophene-2-carbonyl chlorideStructure of 3-Chlorobenzo[b]thiophene-2-carbonyl chloride[21815-91-8]GEO-00658
3-Chlorobenzo[b]thiophene-2-carboxylic acidStructure of 3-Chlorobenzo[b]thiophene-2-carboxylic acid[21211-22-3]GEO-00659
5-ChlorobenzoxazoleStructure of 5-Chlorobenzoxazole[17200-29-2]GEO-00657
2-ChlorobenzoxazoleStructure of 2-Chlorobenzoxazole[615-18-9]GEO-00656
3-ChlorobenzylsulphonamideStructure of 3-Chlorobenzylsulphonamide[89782-88-7]GEO-02549