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352535-83-2
5-Chloro-2-Fluorophenylboronic Acid

Catalog#:1P003N3C

CAS:352535-83-2

MDL:MFCD05664225

Molecular Formula:C6H5BClFO2

Molecular Weight:174.3651

UN Number:

Haz Class:

Packing Group:

Synonyms: 5-Chloro-2-fluorophenylboronic acid; 352535-83-2; ACMC-1AE0A; SCHEMBL246398; CTK4H4096; KS-00000ASP; DTXSID60395469; GGTUVWGMCFXUAS-UHFFFAOYSA-N; ACT07952; BCP15299; ANW-28149; BBL102091; (5-chloro-2-fluorophenyl)boronic acid; SBB071097; STL555890; 5-chloro-2-fluorophenyl boronic acid; AKOS004113770; ZINC169745119; AB22317; AM86895; C2202G1; CS-W003241; EBD2860816; 5-Chloro-2-fluorobenzeneboronic acid; GS-6268; LS11048; QC-4112; RL03324; RTC-068478; TRA-0203471; AK-34816; AN-28715; BC000878; SC-51679; (5-chloro-2-fluoro-phenyl)boronic Acid; SY032671; AB0006256; Boronic acid,B-(5-chloro-2-fluorophenyl)-; DB-029114; ST2402448; TR-049455; 4CH-001238; A6191; FT-0644495; V1933; 5-Chloro-2-FluorophenylboronicAcid; MFCD05664225 (97%); B-8140; 535C832; J-517304; C6H5BClFO2; cc-666; ACN-032820; CID3718925; C2645; 4-AMINO-N-(2,5-DICHLOROPHENYL)BENZAMIDE; MFCD05664225; 5-Chloro-2-fluorobenzeneboronic acid, 97% - 1G 1g; Boronic acid, (5-chloro-2-fluorophenyl)-; PubChem11819; AC1MW5VR;

Keywords: 352535-83-2,MFCD05664225,1P003N3C,5-Chloro-2-Fluorophenylboronic Acid,C6H5BClFO2

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P003N3C 97% 1g $5.00 $4.00 In Stock USA ADD TO CART BUY NOW
1P003N3C 97% 5g $14.00 $11.00 In Stock USA ADD TO CART BUY NOW
1P003N3C 97% 10g $17.00 $13.00 In Stock USA ADD TO CART BUY NOW
1P003N3C 97% 25g $42.00 $32.00 In Stock USA ADD TO CART BUY NOW
1P003N3C 97% 100g $167.00 $126.00 In Stock USA ADD TO CART BUY NOW

  •                                        5-Chloro-2-fluorophenylboronic acid is a versatile building block in chemical synthesis. It is commonly utilized in organic chemistry as a key reagent for Suzuki-Miyaura cross-coupling reactions. This compound serves as a valuable precursor for the introduction of the 5-chloro-2-fluorophenyl group into organic molecules, allowing for the facile synthesis of various biologically and pharmaceutically relevant compounds. Its ability to participate in these coupling reactions enables the efficient formation of carbon-carbon bonds, making it an essential tool for the construction of complex organic molecules in medicinal chemistry and material science applications.
                                        

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