389621-80-1

Basic information

• Product Name: 4-(N,N-DIETHYLAMINOCARBONYL)PHENYLBORONIC ACID
• Synonyms: N,N-DIETHYL 4-BORONOBENZAMIDE;4-[(DIETHYLAMINO)CARBONYL]PHENYLBORONIC ACID;4-(N,N-DIETHYLAMINOCARBONYL)BENZENEBORONIC ACID;4-(N,N-DIETHYLAMINOCARBONYL)PHENYLBORONIC ACID;4-(Diethylcarbamoyl)benzeneboronic acid;Boronic acid, [4-[(diethylamino)carbonyl]phenyl]- (9CI);4-(Diethylcarbonyl)Phenylboron;4-(Diethylcarbamoyl)benzeneboronic acid 98%
• CAS NO: 389621-80-1
• Molecular Formula: C₁₁H₁₆BNO₃
• Molecular Weight: 221.06
• Product Categories: BORONICACID;blocks;BoronicAcids;Boronic acids;Heterocyclic Compounds;Boronic acid;Boronate Ester;Potassium Trifluoroborate
• Mol File: 389621-80-1.mol
• Article Data: 2

Chemical Properties

• Melting Point: 138-142°C
• Boiling Point: 423.3 °C at 760 mmHg
• Flash Point: 209.8 °C
• Appearance: /
• Density: 1.14 g/cm³
• Vapor Pressure: 6.41E-08mmHg at 25°C
• Refractive Index: 1.54
• Storage Temp.: Keep Cold
• Solubility: soluble in Methanol
• PKA: 8.18±0.16(Predicted)
• CAS DataBase Reference: 4-(N,N-DIETHYLAMINOCARBONYL)PHENYLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(N,N-DIETHYLAMINOCARBONYL)PHENYLBORONIC ACID(389621-80-1)
• EPA Substance Registry System: 4-(N,N-DIETHYLAMINOCARBONYL)PHENYLBORONIC ACID(389621-80-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 389621-80-1(Hazardous Substances Data)

Usage

General Description

4-(N,N-Diethylaminocarbonyl)phenylboronic acid is a chemical compound with the molecular formula C14H20BNO3. It is a boronic acid derivative and acts as a reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. 4-(N,N-DIETHYLAMINOCARBONYL)PHENYLBORONIC ACID is commonly used in the Suzuki-Miyaura cross-coupling reaction to form biaryl compounds and has also been utilized in the development of novel pharmaceuticals and materials. 4-(N,N-Diethylaminocarbonyl)phenylboronic acid has potential applications in medicine, proteomics, and polymer science due to its ability to react with a variety of organic and inorganic substrates.

InChI:InChI=1/C11H16BNO3/c1-3-13(4-2)11(14)9-5-7-10(8-6-9)12(15)16/h5-8,15-16H,3-4H2,1-2H3

Upstream product

• 14047-29-1 4-carboxyphenylboronic acid 
• 109-89-7 diethylamine 

Downstream Products

• 911227-51-5 tert-butyl 6-(tert-butyldimethylsilyloxy)-4-(4-(diethylcarbamoyl)phenyl)spiro[chromene-2,4'-piperidine]-1'-carboxylate 
• 911227-81-1 tert-butyl 4-(4-(diethylcarbamoyl)phenyl)-5-(methoxymethoxy)spiro[chromene-2,4'-piperidine]-1'-carboxylate 
• 911227-89-9 C₃₀H₃₈N₂O₄ 
• 911227-92-4 C₃₁H₃₈N₂O₆ 
• 911227-98-0 C₃₂H₄₁N₃O₅ 
• 911228-18-7 C₃₀H₃₈N₂O₄ 
• 911228-30-3 C₂₇H₃₁NO₄ 
• 911228-45-0 benzyl 4-(4-(diethylcarbamoyl)phenyl)-1H-spiro[naphthalene-2,4-piperidine]-1'-carboxylate 
• 911228-62-1 C₂₉H₃₆N₂O₅S 
• 79119-31-6 N, N-diethyl-4-hydroxybenzamide 
• 850175-04-1 N,N-diethyl-4-(2',3',5',6'-tetrahydrospiro[chromene-2,4'-pyran]-4-yl)benzamide 
• 1013334-93-4 C₂₉H₃₆N₂O₄ 
• 1013334-92-3 C₂₈H₃₄N₂O₄ 
• 1013333-37-3 C₃₀H₃₈N₂O₅ 

Relevant articles and documents

11β-HSD1 INHIBITORS

The invention relates to sulfonamide compounds of formula (I) wherein A, B, R1 and Xl to X3 have the meaning as cited in the description and the claims. For example A is biphenyl, B is 3-methoxyphenyl, Rl is H and Xl to X3 are CH. Said compounds are usefu