14559-87-6

Basic information

• Product Name: Boronic acid, (1-methylethenyl)-
• Synonyms: Boronic acid, (1-methylethenyl)-;Prop-1-en-2-ylboronic acid;(1-Methylethenyl)-Boronic acid;Isopropenylboronic Acid;2-Propenylboronic acid;2-Propenylboronic acid Isopropenylboronic acid
• CAS NO: 14559-87-6
• Molecular Formula: C₃H₇BO₂
• Molecular Weight: 85.89748
• Mol File: 14559-87-6.mol
• Article Data: 20

Chemical Properties

• Melting Point: 104℃
• Boiling Point: 78-80℃ (18 Torr)
• Appearance: /
• Density: 0.955±0.06 g/cm3(Predicted)
• Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
• Solubility: DMSO (Slightly), Methanol (Slightly)
• PKA: 9.40±0.43(Predicted)
• Stability: Light and Temperature Sensitive
• CAS DataBase Reference: Boronic acid, (1-methylethenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Boronic acid, (1-methylethenyl)-(14559-87-6)
• EPA Substance Registry System: Boronic acid, (1-methylethenyl)-(14559-87-6)

Safety Data

• Hazardous Substances Data: 14559-87-6(Hazardous Substances Data)

Usage

Uses

Isopropenylboronic Acid is a reagent used in various synthetic preparations.

Upstream product

• 2065-66-9 methyl-triphenylphosphonium iodide 
• 99-90-1 para-bromoacetophenone 
• 1104637-47-9 isopropene boronic acid MIDA ester 
• 5419-55-6 Triisopropyl borate 
• 121-43-7 Trimethyl borate 
• 557-93-7 2-bromoprop-1-ene 
• 7732-18-5 water 
• 13291-18-4 isopropenylmagnesium bromide 
• 14900-40-4 di-n-butyl-(2-propenyl)-boronate 

Downstream Products

• 1041002-74-7 (4R,5R)-2,2-dimethyl-4,5-bis(2-(prop-1-en-2-yl)phenyl)-1,3-dioxolane 
• 1089665-06-4 4,5-dimethoxy-2-(prop-1-en-2-yl)benzaldehyde 
• 1429614-77-6 C₂₅H₁₉N₃NiO₃ 
• 1150263-32-3 methyl 3-bromo-5-(prop-1-en-2-yl)benzoate 
• 1093395-93-7 4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-{[1-(2-isopropenylpyrimidin-4-yl)piperidin-4-yl]methyl}benzamide 
• 942216-07-1 3-isopropenyl-4-methoxy-5-nitrobenzonitrile 
• 1093397-25-1 4-hydroxy-3-nitro-5-[(1E)-prop-1-en-1-yl]benzonitrile 
• 942216-08-2 4-hydroxy-3-isopropenyl-5-nitrobenzonitrile 
• 1415695-77-0 4-(4-(prop-1-en-2-yl)phenyl)thiazol-2-amine 

Relevant articles and documents

Multi-substituted amine compound and its preparation and use (by machine translation)

The invention belongs to the field of medical technology, in particular, the present invention provides the following formula I shown multi-substituted amine compound or its isomer or its pharmaceutically acceptable salt, ester, prodrug or hydrate, its pharmaceutical composition, preparation method thereof and its use in the preparation of medicine for treating aids in use. The compound or pharmaceutical composition containing the compound can be used as an inhibitor for inhibiting HIV integrase with LEDGF/p75 between protein - protein interaction and HIV integrase dimerization, then can be used for the treatment of aids. . (by machine translation)

Copper-Catalyzed Amino Lactonization and Amino Oxygenation of Alkenes Using O-Benzoylhydroxylamines

A copper-catalyzed amino lactonization of unsaturated carboxylic acids has been achieved as well as the analogous intermolecular three-component amino oxygenation of olefins. The transformation features mild conditions and a remarkably broad substrate sco

Tricyclic pyridine derivatives, medicaments containing such compounds, their use and process for their preparation

The present invention relates to compounds defined by formula I wherein the variables R1-R8 are defined as in the description, possessing valuable pharmacological activity. Particularly, the compounds are inhibitors of cholesterol ester transfer protein (CETP) and thus are suitable for treatment and prevention of diseases which can be influenced by inhibition of this enzyme.