Organic acids and derivatives

Organic compounds with acidic properties, and will commonly have carboxylic acids or similar functional groups in their structure. Derived compounds are also included.

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6,586 – 6,600 of 22,188 results

6,586

Frontier Specialty Chemicals 1g, 4-(N-Boc-aminomethyl)phenylboronic acid, 97%, [489446-42-6], A1231 251.09 C12H18BNO4

Compound: 4-(N-Boc-aminomethyl)phenylboronic acid

CAS#: 489446-42-6

MDL#: MFCD04115637

Background: 4-(N-Boc-aminomethyl)phenylboronic acid is a Boc-protected phenylboronic acid used for proteomics research and as a key building block in pharmaceutical and agrochemical synthesis. Its boronic acid functionality supports Suzuki-Miyaura cross-coupling reactions, while the protected amino group enables selective manipulation of specific sites within a molecule during multi-step synthesis.

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6,587

Frontier Specialty Chemicals 5g, Allylboronic acid pinacol ester, 97%, [72824-04-5], A1648 168.05 C9H17BO2

Compound: Allylboronic acid pinacol ester

CAS#: 72824-04-5

MDL#: MFCD00013347

Background: Allylboronic acid pinacol ester is a synthetic specialty chemical useful in the synthesis of pharmaceuticals and specialty organic chemicals. It is commonly used as an allylating reagent in organic synthesis and in transition metal-catalyzed coupling reactions.

Storage: Store at 2-8°C, under dry conditions.

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6,588

Frontier Specialty Chemicals 25g, 3-Aminophenylboronic acid monohydrate, 98%, [206658-89-1], A6087 154.96 C6H8BNO2.H2O

Compound: 3-Aminophenylboronic acid monohydrate

CAS#: 206658-89-1

MDL#: MFCD00149554

Background: An amino-substituted phenylboronic acid used as a reagent for Suzuki-Miyaura cross-coupling. It has been used in the preparation of antivirulence drugs, boronic acid-based beta-lactamase inhibitors, and as a reversible covalent inhibitor of the dopamine transporter in pharmacological research.

Storage: Store at room temperature, under dry conditions.

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6,589

Frontier Specialty Chemicals 5g, 3-Aminophenylboronic acid monohydrate, 98%, [206658-89-1], A6087 154.96 C6H8BNO2.H2O

Compound: 3-Aminophenylboronic acid monohydrate

CAS#: 206658-89-1

MDL#: MFCD00149554

Background: 3-Aminophenylboronic acid monohydrate is an arylboronic acid used as a reagent in Suzuki-Miyaura cross-coupling reactions. It has been used as a boronic acid-based inhibitor of bacterial beta-lactamases, which confer resistance to penicillin and cephem antibiotics. It also serves as a building block for amphiphilic glycopolymers used in glucose-sensing nanoparticles.

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6,590

Frontier Specialty Chemicals 5g, 4-(N-Boc-aminomethyl)phenylboronic acid, 97%, [489446-42-6], A1231 251.09 C12H18BNO4

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6,591

Frontier Specialty Chemicals 25g, Dibenzofuran-4-boronic acid, 97%, [100124-06-9], D5438 212.01 C12H9BO3

Compound: Dibenzofuran-4-boronic acid

CAS#: 100124-06-9

MDL#: not listed

Background: A dibenzofuran-substituted boronic acid used as a Suzuki-Miyaura coupling partner in materials science and pharmaceutical research. Dibenzofuran-containing building blocks are commonly used in the synthesis of organic electronic and photoluminescent materials.

Storage: Store at room temperature, under dry conditions.

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6,592

Frontier Specialty Chemicals 5g, 4-(1-Naphthyl)phenyl boronic acid, 98%, [870774-25-7], N10084 248.084 C16H13BO2

Compound: 4-(1-Naphthyl)phenyl boronic acid

CAS#: 870774-25-7

MDL#: not listed

Background: A naphthyl-substituted phenylboronic acid used as a Suzuki-Miyaura coupling partner in materials science and pharmaceutical research. Naphthyl-biaryl building blocks of this type are commonly used in organic electronic and photoluminescent materials.

Storage: Store at room temperature, under dry conditions.

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6,593

Frontier Specialty Chemicals 1g, Isoquinoline-5-boronic acid, 96%, [371766-08-4], I2102 172.98 C9H8BNO2

Compound: Isoquinoline-5-boronic acid

CAS#: 371766-08-4

MDL#: MFCD03839356

Background: Isoquinoline-5-boronic acid is used in Suzuki-Miyaura cross-coupling reactions pivotal to the formation of carbon-carbon bonds in complex organic molecule synthesis. It serves as a building block in pharmaceutical development targeting cancer and other diseases, and is used in bioconjugation, fluorescent probe development for biological imaging, and advanced materials research.

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6,594

Frontier Specialty Chemicals 25g, 3,5-Dichlorophenylboronic acid, 97%, [67492-50-6], D9266 190.82 C6H5BCl2O2

Compound: 3,5-Dichlorophenylboronic acid

CAS#: 67492-50-6

MDL#: MFCD00051935

Background: 3,5-Dichlorophenylboronic acid is used as an intermediate in pharmaceutical manufacturing and plays a role in Suzuki-Miyaura cross-coupling reactions essential for developing active pharmaceutical ingredients. It is also a reactant in trifluoromethylation, intramolecular aromatic carbenoid insertion, and cyanation reactions for synthesizing aromatic nitriles. It has additionally been used to facilitate transport of ribonucleosides across liposome membranes in biophysical research.

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6,595

Frontier Specialty Chemicals 5g, Isoquinoline-5-boronic acid, 96%, [371766-08-4], I2102 172.98 C9H8BNO2

Pricing & Availability

6,596

Frontier Specialty Chemicals 5g, Cyclopropylboronic acid pinacol ester, 98%, [126689-01-8], C1471 168.05 C9H17BO2

Compound: Cyclopropylboronic acid pinacol ester

CAS#: 126689-01-8

MDL#: MFCD05663847

Background: A cyclopropyl boronic ester used as a stable coupling partner in Suzuki-Miyaura cross-coupling reactions to install cyclopropyl groups onto aromatic and heteroaromatic scaffolds. It has been applied in the synthesis of FLAP inhibitors and other pharmaceutically relevant compounds.

Storage: Store at 2-8°C, under dry conditions.