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3,4-Dimethoxyphenylboronic acid(contains varying amounts of Anhydride) - 97%, high purity , CAS No.122775-35-3
Basic Description Synonyms EN300-52543 | D3512 | FT-0614338 | 3,4-Dimethoxyphenylboronic aicd | MFCD01074574 | 3,4-Dimethoxyphenylboronicacid | 4,5-dimethoxyphenylboronic acid | (3,4-dimethoxyphenyl)boronic acid | (3,4-dimethoxyphenyl)-boronic acid | 3,4-Dimethoxyphenylboronic acid Specifications & Purity ≥97% Storage Temp Store at 2-8°C Shipped In Wet ice Product Description
application:
3,4-Dimethoxyphenylboronic acid can be used: As a substrate in the cross-coupling reaction with 5,7-dichloropyrido[4,3-d]pyrimidine catalyzed by palladium. As a starting material for the synthesis of buflavine 1, a natural alkaloid. In one of the key synthetic steps for the preparation of lipidated malarial glycosylphosphatidylinositols (GPI) disaccharide. To prepare 3,3″,4,4″-tetramethoxy-1,1′:4′,1″-terphenyl by reacting with 1,4-dibromobenzene using Pd catalyst.
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References The page will load shortly, Thanks for your patience!
Names and Identifiers Pubchem Sid 504761186 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504761186 IUPAC Name (3,4-dimethoxyphenyl)boronic acid INCHI InChI=1S/C8H11BO4/c1-12-7-4-3-6(9(10)11)5-8(7)13-2/h3-5,10-11H,1-2H3 InChi Key RCVDPBFUMYUKPB-UHFFFAOYSA-N Canonical SMILES B(C1=CC(=C(C=C1)OC)OC)(O)O Isomeric SMILES B(C1=CC(=C(C=C1)OC)OC)(O)O WGK Germany 3 PubChem CID 2734702 Molecular Weight 181.98 Reaxy-Rn 5334877
Certificates(CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Soluble in water (25 g/L). Melt Point(°C) 245-250°C Molecular Weight 181.980 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 3 Exact Mass 182.075 Da Monoisotopic Mass 182.075 Da Topological Polar Surface Area 58.900 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 153.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
Safety and Hazards(GHS) Pictogram(s) GHS07 Signal Warning Hazard Statements H315: Causes skin irritation
H319: Causes serious eye irritation
H335: May cause respiratory irritation
Precautionary Statements P261: Avoid breathing dust/fume/gas/mist/vapors/spray.
P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.
P280: Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352: IF ON SKIN: wash with plenty of water.
P321: Specific treatment (see ... on this label).
P405: Store locked up.
P501: Dispose of contents/container to ...
P264: Wash hands [and …] thoroughly after handling.
P271: Use only outdoors or in a well-ventilated area.
P304+P340: IF INHALED: Remove person to fresh air and keep comfortable for breathing.
P403+P233: Store in a well-ventilated place. Keep container tightly closed.
P362+P364: Take off contaminated clothing and wash it before reuse.
P264+P265: Wash hands [and …] thoroughly after handling. Do not touch eyes.
P337+P317: If eye irritation persists: Get medical help.
P332+P317: If skin irritation occurs: Get medical help.
P319: Get medical help if you feel unwell.
WGK Germany 3 Reaxy-Rn 5334877
Citations of This Product (1 ) 1. Feng Ouyang, Xiaoli Zhang, Tao Wang, Qi Shuai. (2022) A fluorescent turn on/off probe for glucose detection based on a boronic acid-capped 1,1′-ferrocenedicarboxylic acid functional graphene oxide. Materials Today Communications, 33 (104681). [PMID: ] [10.1016/j.mtcomm.2022.104681 ]
References 1. Feng Ouyang, Xiaoli Zhang, Tao Wang, Qi Shuai. (2022) A fluorescent turn on/off probe for glucose detection based on a boronic acid-capped 1,1′-ferrocenedicarboxylic acid functional graphene oxide. Materials Today Communications, 33 (104681). [PMID: ] [10.1016/j.mtcomm.2022.104681 ]
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