4-Chlorophenylboronic acid

Product Details

CAS No:1679-18-1

MF:C6H6BClO2

Appearance:white or off-white crystalline powder

Specification:98.5%

UN number:-

Package:1/5/10/25kgs/drum

Supply Capacity:MT

Synonyms:4-Chlorophenylboronic acid,97%;4-Chlorophenylboronic acid, May contain varying amounts of anhydride, 97%;4-Chlorophenylboronic acid,4-Chlorobenzeneboronic acid;p-chlorophenylboronic aci;(4-chlorophenyl)boronic acid(SALTDATA: 0.7H2O);4-Chlorophenylboronic acid, 97% 5GR;NSC 25408;BORONIC ACID, (4-CHLOROPHENYL)-;P-CHLOROBENZENEBORONIC ACID;; 4-Chlorophenylboronic acid; 1679-18-1; (4-chlorophenyl)boronic acid; p-Chlorophenylboronic acid; Boronic acid, (4-chlorophenyl)-; p-Chlorobenzeneboronic acid; Benzeneboronic acid, p-chloro-; Boronic acid, p-chlorophenyl; (p-Chlorophenyl)metaboric acid; NSC 25408; EINECS 216-845-5; AB2T8N4T4C; BRN 2936346; AI3-32764; (P-CHLOROPHENYL)BORONIC ACID; NSC-25408; 4-16-00-01667 (Beilstein Handbook Reference); B-(4-CHLOROPHENYL)BORONIC ACID; DTXSID50168427; BORONIC ACID, B-(4-CHLOROPHENYL)-; RefChem:522049; DTXCID0090918; 216-845-5; 4-Chlorobenzeneboronic acid; MFCD00039137; 4-chlorophenyl boronic acid; 4-Chlorophenylboronicacid; 4-chloro-phenylboronic acid; (4-chloro-phenyl)-boronic acid; [4-chloro-phenyl]-boronic acid; 4-chloro phenyl boronic acid; (4-chlorophenyl)dihydroxyborane; 4-Chloroboronic acid; B-(4-CHLOROPHENYL)-BORONIC ACID; Vismodegib Impurity 11; 4chlorophenylboronic acid; Phenylboronic acid, 18; 4-chlorophenyboronic acid; 4-chlorphenylboronic acid; 4-chorophenylboronic acid; WLN: QBQR DG; 4chlorophenyl boronic acid; p-chloro phenylboronic acid; p-chlorophenyl boronic acid; UNII-AB2T8N4T4C; (4-chlorophenyl)boronicacid; 4-chlorophenyl-boronic acid; para-chlorophenylboronic acid; 4-chloro-benzeneboronic acid; 4-chlorobenzene boronic acid; SCHEMBL28166; 4- chlorophenyl boronic acid; 4-chloro-phenyl boronic acid; 4-chloro benzene boronic acid; (4-chloro-phenyl)boronic acid; (4-chlorophenyl) boronic acid; CHEMBL1209679; BDBM92725; 4-Chlorophenylboronic acid, 95%; ALBB-006093; CS-D1133; NSC25408; EBC-03137; SBB048060; AKOS000121904; AB01763; AC-3320; AS-2333; FC08281; NCGC00249500-01; SY004529; DB-031707; NS00025512; EN300-29827; F010986; F9995-0588; Z295122658; 4-Chlorobenzeneboronic Acid (contains varying amounts of Anhydride); 4-Chlorophenylboronic Acid (contains varying amounts of Anhydride); 4-Chlorophenylboronic acid(contains varying amounts of Anhydride)

Product application:4-Chlorophenylboronic acid,1679-18-1,4-Chloro-benzeneboronic acid,p-Chlorophenylboronic acid,4-Chlorobenzeneboronic acid,Arylboronic acid building block,Suzuki coupling reagent,Suzuki-Miyaura cross-coupling reactant,C-C bond formation synthon,Pharmaceutical grade 4-Chlorophenylboronic acid,Targeted oncology API intermediate,Antihypertensive drug intermediate,Boscalid fungicide intermediate,Crop protection chemical building block,OLED intermediate,Organic optoelectronic material monomer,Conjugated polymer building block,Functional polymer crosslinker,Fine organic chemical intermediate,High purity 4-Chlorophenylboronic acid 99%,4-Chlorophenylboronic acid manufacturer China,CAS 1679-18-1 supplier,Suzhou Health Chemicals organoboron,4-Chlorophenylboronic acid wholesale bulk export

 

4-Chlorophenylboronic acid serves as an indispensable, high-purity arylboronic acid building block, premier Suzuki-Miyaura cross-coupling nucleophilic reagent, and versatile synthetic intermediate extensively utilized across targeted biopharmaceuticals, active pharmaceutical ingredient (API) manufacturing, sustainable crop protection chemistry, organic optoelectronics, and advanced materials engineering sectors. In medicinal chemistry and commercial pharmaceutical manufacturing, it represents a foundational benchmark synthon for executing palladium-catalyzed Suzuki-Miyaura cross-coupling transformations with aromatic halides, triflates, and tosylates under mild, functional-group-tolerant conditions; by facilitating the clean, high-yielding formation of substituted biaryl and aryl-heteroaryl architectures, it is globally employed to assemble essential rigid pharmacophores for targeted kinase inhibitors, antineoplastic therapeutics, angiotensin receptor blockers, antiviral agents, and cardiovascular therapies. In agrochemical science and sustainable crop protection, this compound functions as the irreplaceable core raw material for the commercial multi-ton synthesis of Boscalid, a blockbuster succinate dehydrogenase inhibitor (SDHI) fungicide widely applied to control Botrytis cinerea, Sclerotinia, and powdery mildew across valuable horticultural crops, oilseeds, and cereals. In organic semiconductors and photonic display technologies, it is utilized as an essential aryl building block for constructing high-efficiency OLED fluorescent and phosphorescent emitters, bipolar charge-transport layers, and conjugated polymers for organic photovoltaics. In specialty polymer engineering and smart biomaterials, its boronic acid moiety is deployed to synthesize reversible covalent boronate-ester crosslinked self-healing networks, glucose-responsive biosensing hydrogels, and high-temperature poly(arylene) resins. In functional adhesives, automotive high-durability coatings, and specialized elastomeric materials, it acts as a coupling modifier that enhances cohesive strength and interfacial substrate anchoring. Furthermore, in specialized textile functional finishes, leather protective coatings, eco-friendly wood preservatives, and metallurgical corrosion inhibition additives for petroleum and natural gas pipelines, chemical architectures engineered from 4-Chlorophenylboronic acid deliver outstanding bond-forming reliability, structural versatility, and broad multi-industry performance.