TERT-BUTYL 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CYCLOHEX-3-ENYLCARBAMATE - Names and Identifiers
Name | 2-Methyl-2-propanyl [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-cyclohexen-1-yl]carbamate
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Synonyms | 4-Boc-amino-cyclohex-1-enyl-boronic acid pinacol ester 4-(Boc-amino)-1-cyclohexene-1-boronic Acid Pinacol Ester (4-((TERT-BUTOXYCARBONYL)AMINO)CYCLOHEX-1-EN-1-YL)BORONIC ACID PINACOL ESTER tert-butyl N-[4-(tetraMethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-en-1-yl]carbaMate tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-enylcarbamate TERT-BUTYL 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CYCLOHEX-3-ENYLCARBAMATE tert-Butyl (4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-en-1-yl)carbaMate 2-Methyl-2-propanyl [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-cyclohexen-1-yl]carbamate
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CAS | 1251732-64-5
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InChI | InChI=1S/C17H30BNO4/c1-15(2,3)21-14(20)19-13-10-8-12(9-11-13)18-22-16(4,5)17(6,7)23-18/h8,13H,9-11H2,1-7H3,(H,19,20) |
TERT-BUTYL 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CYCLOHEX-3-ENYLCARBAMATE - Physico-chemical Properties
Molecular Formula | C17H30BNO4
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Molar Mass | 323.24 |
Density | 1.03±0.1 g/cm3(Predicted) |
pKa | 12.50±0.40(Predicted) |
Storage Condition | Inert atmosphere,Store in freezer, under -20°C |
Sensitive | Irritant |
Refractive Index | 1.483 |
MDL | MFCD12032216 |
TERT-BUTYL 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CYCLOHEX-3-ENYLCARBAMATE - Introduction
tert-Butyl 4-(4,4, 5,5-tetramethyl -1,3, 2-dioxaborolan-2-yl) cyclohex-3-enyl carbamate, also known as BCN ester, is an organic compound. The following is an introduction to its nature, use, preparation and safety information:
Nature:
BCN ester is a colorless liquid with a low boiling point and flash point. It is stable and can be stored for a long time at room temperature. It decomposes under the action of oxidants.
Use:
BCN ester is an important chemical reagent and intermediate. It can be used to synthesize various organic compounds, such as drugs, pesticides, dyes and polymer materials. BCN esters can also be used as crosslinkers in organic synthesis to improve the physical and chemical properties of materials.
Method:
The preparation of BCN esters is generally achieved by chemical reaction steps. A common synthetic method is the reaction of 1,3-dichloro-2-boropentane and an ester of tetramethylborohydride or tetramethylboronic acid to give the target compound.
Safety Information:
BCN esters are not particularly hazardous under normal conditions of use. However, as a chemical substance, it is still necessary to comply with relevant safety procedures when used. If wearing chemical protective gloves and goggles, avoid direct contact with skin and eyes. Be careful to avoid fire and high temperature during operation. Please store it in a dry, well-ventilated place, away from fire and flammable materials. In the case of accidental spills, appropriate measures are required for removal and disposal.
Last Update:2024-04-09 20:45:29