489446-42-6

Basic information

• Product Name: 4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID
• Synonyms: 4-(Aminomethyl)benzeneboronicacid,N-BOCprotected97%;4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID;4-(AMINOMETHYL)BENZENEBORONIC ACID, N-BOC PROTECTED;4-(TERT-BUTOXYCARBONYLAMINOMETHYL)PHENYLBORONIC ACID;4-(Aminomethyl)benzeneboronic acid, N-BOC protected 97%;N-BOC-4-(AMINOMETHYL)BENZENEBORONIC ACID;4-(Boc-aMinoMethyl)benzeneboronic acid, 97%;[4-[[(2-methylpropan-2-yl)oxycarbonylamino]methyl]phenyl]boronic acid
• CAS NO: 489446-42-6
• Molecular Formula: C₁₂H₁₈BNO₄
• Molecular Weight: 251.09
• Product Categories: Boronate Ester;Boronic Acid;Potassium Trifluoroborate;blocks;BoronicAcids;Amino;Aryl;Organoborons
• Mol File: 489446-42-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 208-210°C
• Appearance: /
• Density: 1.15 g/cm³
• Refractive Index: 1.526
• Storage Temp.: Keep Cold
• PKA: 8.54±0.16(Predicted)
• CAS DataBase Reference: 4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID(489446-42-6)
• EPA Substance Registry System: 4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID(489446-42-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• WGK Germany: 3
• Hazardous Substances Data: 489446-42-6(Hazardous Substances Data)

Usage

Description

4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID, also known as 4-(Boc-aminomethyl)benzeneboronic acid, is a chemical compound characterized by the presence of a boronic acid functional group and a protected amino group. This molecule is known for its ability to form reversible covalent bonds with diols, making it a versatile building block in various applications.

Uses

Used in Biomimetic Membranes:
4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID is used as a key component in the preparation of lipid pore-filled silica thin-film membranes. These membranes are designed for the biomimetic recovery of diluted carbohydrates, leveraging the selective binding properties of the boronic acid group to target specific carbohydrate molecules.
Used in Proteomics Research:
In the field of proteomics, 4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID serves as a valuable reagent for the study of proteins and their interactions. 4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID's boronic acid functionality allows for the selective capture and analysis of glycoproteins, which are proteins with attached carbohydrate moieties. This selective binding is crucial for the identification and characterization of glycoproteins in complex biological samples.

InChI:InChI=1/C12H18BNO4/c1-12(2,3)18-11(15)14-8-9-4-6-10(7-5-9)13(16)17/h4-7,16-17H,8H2,1-3H3,(H,14,15)

Upstream product

• 87199-17-5 4-formylphenylboronic acid, 
• 4248-19-5 tert-butyl carbazate 
• 24424-99-5 di-tert-butyl dicarbonate 
• 51239-46-4 4-(aminomethyl)phenylboronic acid 

Downstream Products

• 945241-81-6 1-(benzo[d][1,3]dioxol-5-yl)-N-(6-methyl-4'-(propylsulfonamidomethyl)biphenyl-3-yl)cyclopropanecarboxamide 
• 945240-16-4 1-(benzo[d][1,3]dioxol-5-yl)-N-(6-methyl-4'-(propionamidomethyl)biphenyl-3-yl)cyclopropanecarboxamide 
• 945235-39-2 N-(4′-(aminomethyl)-6-methylbiphenyl-3-yl)-1-(benzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamide 
• 1380500-86-6 tert-butyl N-{[4-(6-methyl-1,2,4,5-tetrazin-3-yl)phenyl]methyl}carbamate 
• 943153-49-9 [4-(5-fluoro-2-methoxy-pyridin-3-yl)-benzyl]-carbamic acid-tert-butyl ester 
• 928650-36-6 N-(tert-butoxycarbonyl)-4-[5-(3,3-dimethylbutyryl)thiophen-2-yl]-benzylamine 
• 928650-31-1 4-[2-(cyclopropylmethyl-amino)-pyrimidin-4-yl]-N-(tert-butoxycarbonyl)-benzylamine 
• 928650-25-3 4-[4-(cyclopropylmethyl-amino)-pyrimidin-2-yl]-N-(tert-butoxycarbonyl)-benzylamine 
• 928650-19-5 4-[6-(cyclopropylmethyl-amino)-pyrimidin-4-yl]-N-(tert-butoxycarbonyl)-benzylamine 
• 2115897-23-7 (2S,4R)-1-[(2S)-2-amino-3,3-dimethylbutanoyl]-4-hydroxy-N-[[4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide hydrochloride 

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