Thiophenes

Aobchem Dibenzo[b d]thiophene-2-carboxylic acid | ≥97% | CAS 20928-05-6 | C13H8O2S | 1g

Dibenzo[b d]thiophene-2-carboxylic acid | ≥97% | CAS 20928-05-6 | C13H8O2S | 1g

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Aobchem Tert-butyl 5-bromothiophene-2-carboxylate | ≥95% | CAS 62224-20-8 | C9H11BrO2S | 5g

Tert-butyl 5-bromothiophene-2-carboxylate | ≥95% | CAS 62224-20-8 | C9H11BrO2S | 5g

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Aobchem 4-Chloro-3-thiophenecarboxylic acid | ≥95% | CAS 59337-81-4 | C5H3ClO2S | 500mg

4-Chloro-3-thiophenecarboxylic acid | ≥95% | CAS 59337-81-4 | C5H3ClO2S | 500mg

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Aobchem Dibenzo[b d]thiophene-2-carboxylic acid | ≥97% | CAS 20928-05-6 | C13H8O2S | 5g

Dibenzo[b d]thiophene-2-carboxylic acid | ≥97% | CAS 20928-05-6 | C13H8O2S | 5g

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Aobchem Ethyl 4-bromothiophene-3-carboxylate | ≥97% | CAS 224449-33-6 | C7H7BrO2S | 250mg

Ethyl 4-bromothiophene-3-carboxylate | ≥97% | CAS 224449-33-6 | C7H7BrO2S | 250mg

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Aobchem Ethyl 4-bromothiophene-3-carboxylate | ≥97% | CAS 224449-33-6 | C7H7BrO2S | 1g

Ethyl 4-bromothiophene-3-carboxylate | ≥97% | CAS 224449-33-6 | C7H7BrO2S | 1g

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Aobchem 4-Bromothiophene-3-carboxamide | ≥97% | CAS 100245-61-2 | C5H4BrNOS | 5g

4-Bromothiophene-3-carboxamide | ≥97% | CAS 100245-61-2 | C5H4BrNOS | 5g

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Aobchem Ethyl 3-bromothiophene-2-carboxylate | ≥97% | CAS 62224-14-0 | C7H7BrO2S | 250mg

Ethyl 3-bromothiophene-2-carboxylate | ≥97% | CAS 62224-14-0 | C7H7BrO2S | 250mg

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eMolecules​ 16694-17-0 | 4-Bromothiophene-3-carboxylic acid | Ambeed | MFCD01233020 | 207.040 | C5H3BrO2S | 98.000 | OC(=O)c1cscc1Br | 250mg | 552646715

4-Bromothiophene-3-carboxylic acid | Ambeed | 16694-17-0 | MFCD01233020 | 207.040 | C5H3BrO2S | 98.000 | OC(=O)c1cscc1Br | 250mg | 552646715

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eMolecules​ 16694-17-0 | 4-Bromothiophene-3-carboxylic acid | Ambeed | MFCD01233020 | 207.040 | C5H3BrO2S | 98.000 | OC(=O)c1cscc1Br | 1g | 552646717

4-Bromothiophene-3-carboxylic acid | Ambeed | 16694-17-0 | MFCD01233020 | 207.040 | C5H3BrO2S | 98.000 | OC(=O)c1cscc1Br | 1g | 552646717

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Medchemexpress LLC 3-Bromothiophene | 872-31-1 | 99.8% | C4H3BrS | 10 G

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3-Bromothiophene is a bromine atom-substituted 3-halogenated thiophene. Its polymers are conductive polymers with potential optoelectronic application value. It also serves as a key intermediate in the synthesis of various important pharmaceuticals, agrochemicals, and cosmetics. Additionally, 3-Bromothiophene can be used to synthesize chalcones and their derivatives, some of which demonstrate excellent anti-inflammatory, analgesic, and antibacterial activities.

• Bromine atom-substituted 3-halogenated thiophene
• Polymers are conductive with potential optoelectronic application value
• Key intermediate in synthesis of pharmaceuticals, agrochemicals, and cosmetics
• Used to synthesize chalcones and their derivatives
• Derivatives demonstrate anti-inflammatory, analgesic, and antibacterial activities

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eMolecules​ 16694-17-0 | 4-Bromothiophene-3-carboxylic acid | Combi-Blocks | MFCD01233020 | 207.040 | C5H3BrO2S | 97.000 | OC(=O)c1cscc1Br | 25g | 350782544

4-Bromothiophene-3-carboxylic acid | Combi-Blocks | 16694-17-0 | MFCD01233020 | 207.040 | C5H3BrO2S | 97.000 | OC(=O)c1cscc1Br | 25g | 350782544

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eMolecules​ 16694-17-0 | 4-Bromo-thiophene-3-carboxylic acid | J & W PharmLab LLC | MFCD01233020 | 207.040 | C5H3BrO2S | 96.000 | OC(=O)c1cscc1Br | 25g | 452547839

4-Bromo-thiophene-3-carboxylic acid | J & W PharmLab LLC | 16694-17-0 | MFCD01233020 | 207.040 | C5H3BrO2S | 96.000 | OC(=O)c1cscc1Br | 25g | 452547839

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eMolecules​ 16694-17-0 | 4-bromothiophene-3-carboxylic acid | Pharmablock | MFCD01233020 | 207.040 | C5H3BrO2S | 97.000 | OC(=O)c1cscc1Br | 2.5g | 686929394

4-bromothiophene-3-carboxylic acid | Pharmablock | 16694-17-0 | MFCD01233020 | 207.040 | C5H3BrO2S | 97.000 | OC(=O)c1cscc1Br | 2.5g | 686929394

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Medchemexpress LLC Azido-peg2-hydrazide-boc | 2100306-56-5 | MFCD30828695 | 95% | C12H23N5O5 | 100 MG

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Azido-PEG2-hydrazide-Boc is a PEG-based PROTAC linker used in the synthesis of PROTACs. It acts as a click chemistry reagent, featuring an azide group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. It can also participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups.

• Utilized in PROTAC synthesis
• Functions as a click chemistry reagent
• Contains an azide group
• Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions
• Can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions

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