871333-99-2

Basic information

• Product Name: (1S)-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPT-2-EN-2-YLBORONIC ACID
• Synonyms: (1S)-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPT-2-EN-2-YLBORONIC ACID;(1S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-en-2-ylboronic acid 95%;(1S)-1,7,7-Trimethylbicyclo[2.2.1)hept-2-en-2-ylboronic;(1S)-1,7,7-TriMethylnorborn-2-ene-2-boronic acid, 95%;[(1S)-1,7,7-Trimethylnorborn-2-en-2-yl]boronic acid, (1S)-2-Borono-1,7,7-trimethylbicyclo[2.2.1]hept-2-ene;[(1S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-en-2-yl]boronicacid95%
• CAS NO: 871333-99-2
• Molecular Formula: C₁₀H₁₇BO₂
• Molecular Weight: 180.05
• Product Categories: blocks;BoronicAcids
• Mol File: 871333-99-2.mol

Chemical Properties

• Melting Point: 205-207
• Boiling Point: 283.3°C at 760 mmHg
• Flash Point: 125.1°C
• Appearance: /
• Density: 1.07g/cm³
• Vapor Pressure: 0.000373mmHg at 25°C
• Refractive Index: 1.511
• Storage Temp.: Keep Cold
• CAS DataBase Reference: (1S)-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPT-2-EN-2-YLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (1S)-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPT-2-EN-2-YLBORONIC ACID(871333-99-2)
• EPA Substance Registry System: (1S)-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPT-2-EN-2-YLBORONIC ACID(871333-99-2)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 871333-99-2(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(1S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-en-2-ylboronic acid is used as a reagent in organic synthesis for its ability to form reversible covalent complexes with other molecules. This characteristic makes it a versatile building block for creating a variety of complex organic structures.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (1S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-en-2-ylboronic acid is employed as a key intermediate in the synthesis of potential drug candidates. Its ability to interact with various biological molecules through reversible covalent bonding can be harnessed to develop new therapeutic agents with improved efficacy and selectivity.
Used in Drug Delivery Systems:
(1S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-en-2-ylboronic acid can be utilized in the development of drug delivery systems, where its reversible covalent bonding properties can be exploited to enhance the delivery, bioavailability, and therapeutic outcomes of various pharmaceuticals. This application can be particularly beneficial in improving the efficacy of drugs with poor solubility or stability.
Used in Chemical Research:
(1S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-en-2-ylboronic acid serves as a valuable research tool in chemical research, where its unique bonding properties can be studied to gain insights into the mechanisms of molecular recognition and interactions. This understanding can contribute to the advancement of chemical sciences and the development of novel materials and compounds.

InChI:InChI=1/C10H17BO2/c1-9(2)7-4-5-10(9,3)8(6-7)11(12)13/h6-7,12-13H,4-5H2,1-3H3/t7?,10-/m0/s1

Downstream Products

• 1142225-50-0 methyl 2'-fluoro-5'-(methyloxy)-2-((1R,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-en-2-yl)-1,1'-biphenyl-4-carboxylate