- Product Details
Keywords
- Pyridin-4-boronic acid
- 1692-15-5
- 98% purity
Quick Details
- ProName: Pyridin-4-boronic acid
- CasNo: 1692-15-5
- Molecular Formula: C5H6BNO2
- Appearance: powder
- Application: intermediate
- DeliveryTime: in stock
- PackAge: accroding to the need
- Port: Shanghai Port
- ProductionCapacity: 100 Kilogram/Day
- Purity: 98% purity
- Storage: Sealed in dry,Room Temperature
- Transportation: air,sea and courier
- LimitNum: 1 Gram
- Grade: Industrial Grade,Pharma Grade,Electron...
Superiority
Product Name: Pyridine-4-boronic acid
Synonyms: PYRIDYL-4-BORONIC ACID;PYRIDINE-4-BORONIC ACID;PYRIDINE-4-BORONIC ACID HYDRATE;PYRIDIN-4-YLBORONIC ACID;PYRIDIN-4-YL-4-BORONIC ACID;RARECHEM AH PB 0240;TIMTEC-BB SBB004280;AKOS BRN-0273
CAS: 1692-15-5
MF: C5H6BNO2
MW: 122.92
EINECS: 671-679-4
Mol File: 1692-15-5.mol
Details
Melting point >300 °C (lit.)
Boiling point 308.8±34.0 °C(Predicted)
density 1.22±0.1 g/cm3(Predicted)
storage temp. -20°C
pka 7.59±0.10(Predicted)
BRN 471944
InChIKey QLULGIRFKAWHOJ-UHFFFAOYSA-N
CAS DataBase Reference 1692-15-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi,C,F
Risk Statements 36/37/38-22-34-11
Safety Statements 22-24/25-36/37/39-26-45-16
WGK Germany 3
Hazard Note Irritant
HazardClass IRRITANT, KEEP COLD
HS Code 29339900
MSDS Information
Provider Language
SigmaAldrich English
ACROS English
ALFA English
Pyridine-4-boronic acid Usage And Synthesis
Uses
Pyridine-4-boronic acid can be used as a candidate for Suzuki-Miyaura coupling reaction. Especially, as a N-containing building blocks, pyridine-4-boronic acid was employed to construct some heterocyclic compounds with superior biological activities.
Description Pyridine-4-boronic acid is a kind of boronic acid derivative. It is useful building blocks in crystal engineering. It can also be used as a catalyst to act as a dehydrative condensation agent to synthesize amides using carboxylic acid and amines as raw materials. Its derivative, polystyrene-bound 4-pyridineboronic acid, is a useful catalyst for amidation reaction and esterification of alpha-hydrocarboxylic acids.
Chemical Properties light orange granular powder
Uses suzuki reaction
Uses Boronic acid derivatives and their binding affinities with diols.
References #
José J. CamposGaxiola et al. "Pyridineboronic Acids as Useful Building Blocks in Combination with Perchloroplatinate(II) and -(IV) Salts: 1D, 2D, and 3D Hydrogen-Bonded Networks Containing X-H•••Cl2Pt− (X = C, N+), B(OH)2•••Cl2Pt−, and B(OH)2•••(HO)2B Synthons." Crystal Growth & Design 10.7(2010).
Kara, H., A. G. Orpen, and T. J. Podesta. "Pyridine boronic acids as building blocks in crystal engineering." Acta Crystallographica 61.Suppl (2001): C357.
Pyridine-4-boronic acid Preparation Products And Raw materials
Preparation Products 3-PYRIDIN-4-YL-BENZOIC ACID-->Paraquat dichloride-->PYRIDINE, 4,4'-[1,1'-BIPHENYL]-4,4'-DIYLBIS--->2-(4-Pyridyl)benzaldehyde-->1,4-bis(pyrid-4-yl)benzene-->4-(5-isopropoxy-2-Methyl-4-nitrophenyl)pyridine-->PIPERIDINE-4-BORONIC ACID-->4-Phenylpyridine