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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.

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  • 489446-42-6 Structure
  • Basic information

    1. Product Name: 4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID
    2. 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
    3. CAS NO:489446-42-6
    4. Molecular Formula: C12H18BNO4
    5. Molecular Weight: 251.09
    6. EINECS: N/A
    7. Product Categories: Boronate Ester;Boronic Acid;Potassium Trifluoroborate;blocks;BoronicAcids;Amino;Aryl;Organoborons
    8. Mol File: 489446-42-6.mol
  • Chemical Properties

    1. Melting Point: 208-210°C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.15 g/cm3
    6. Refractive Index: 1.526
    7. Storage Temp.: Keep Cold
    8. Solubility: N/A
    9. PKA: 8.54±0.16(Predicted)
    10. CAS DataBase Reference: 4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID(489446-42-6)
    12. EPA Substance Registry System: 4-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID(489446-42-6)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 489446-42-6(Hazardous Substances Data)

489446-42-6 Usage

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.

Check Digit Verification of cas no

The CAS Registry Mumber 489446-42-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,9,4,4 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 489446-42:
(8*4)+(7*8)+(6*9)+(5*4)+(4*4)+(3*6)+(2*4)+(1*2)=206
206 % 10 = 6
So 489446-42-6 is a valid CAS Registry Number.
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)

489446-42-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H53225)  4-(Boc-aminomethyl)benzeneboronic acid, 97%   

  • 489446-42-6

  • 250mg

  • 364.0CNY

  • Detail
  • Alfa Aesar

  • (H53225)  4-(Boc-aminomethyl)benzeneboronic acid, 97%   

  • 489446-42-6

  • 1g

  • 1457.0CNY

  • Detail

489446-42-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[[(2-methylpropan-2-yl)oxycarbonylamino]methyl]phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names 4-(Aminomethyl)benzeneboronic acid,N-BOC protected

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:489446-42-6 SDS

489446-42-6Downstream Products

489446-42-6Relevant articles and documents

Design, synthesis and biological evaluation of PSMA/hepsin-targeted heterobivalent ligands

Subedi, Milan,Minn, Il,Chen, Jianbo,Kim, YunHye,Ok, Kiwon,Jung, Yong Woo,Pomper, Martin G.,Byun, Youngjoo

, p. 208 - 218 (2016)

Cell surface biomarkers such as prostate-specific membrane antigen (PSMA) and hepsin have received considerable attention as targets for imaging prostate cancer (PCa) due to their high cell surface expression in such tumors and easy access for imaging pro

Synthesis method of 4-amino methylphenylboronic acid hydrochloride

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Paragraph 0020; 0022; 0024; 0026; 0028; 0030, (2021/04/28)

The invention discloses a synthesis method of 4-amino methylphenylboronic acid hydrochloride, and belongs to the field of organic synthesis. According to the method, 4-formyl phenylboronic acid is used as an initial raw material and is condensed with tert-butyl carbamate, and the 4-amino methylphenylboronic acid hydrochloride is generated through three steps of reactions of reduction and Boc removal. According to the method, imine is synthesized through condensation with 4-formyl phenylboronic acid, then sodium borohydride is reduced, and finally deprotection and salification are carried out, so that direct high-pressure hydrogenation in literatures is avoided, the yield is obviously increased, and meanwhile, the process reproducibility is good.

QUINOXALINE COMPOUNDS AND USES THEREOF

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Paragraph 00273, (2015/11/09)

This invention provides compounds of formula I and subsets thereof: wherein T, J, R, R4, Rq, o, RA, and RB and subsets thereof are as described in the specification. The compounds are inhibitors of NAMPT and are thus useful for treating cancer, inflammatory conditions, or T-cell mediated autoimmune disease.

Compounds with medicinal effects due to interaction with the glucocorticoid receptor

-

Page/Page column 17, (2010/11/27)

The invention provides for compounds having the structure according to the formula I

Small molecule thienopyrimidine-based protein tyrosine kinase inhibitors

-

Page/Page column 40, (2010/02/15)

Various thienopyrimidine-based analog compounds are able to selectively inhibit the Src family of tyrosine kinases. These compounds are useful in the treatment of various diseases including hyperproliferative diseases, hematologic diseases, osteoporosis, neurological diseases, autoimmune diseases, allergic/immunological diseases, or viral infections.

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