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865869-26-7

4,4,5,5-Tetramethyl-2-(4-methylcyclohex-1-enyl)-1,3,2-dioxaborolane is a dioxaborolane derivative, a class of compounds widely used in organic synthesis and catalysis. This specific compound features a dioxaborolane ring with four methyl groups and a 4-methylcyclohex-1-enyl substituent, making it a versatile reagent in organic reactions.
Used in Organic Synthesis:
4,4,5,5-Tetramethyl-2-(4-methylcyclohex-1-enyl)-1,3,2-dioxaborolane is used as a reagent for facilitating the synthesis of complex organic molecules. Its unique structure allows it to participate in various organic reactions, contributing to the formation of carbon-carbon bonds and the creation of intricate molecular architectures.
Used in Suzuki Coupling Reactions:
In the field of organic chemistry, 4,4,5,5-Tetramethyl-2-(4-methylcyclohex-1-enyl)-1,3,2-dioxaborolane is used as a boron-containing component in Suzuki coupling reactions. It plays a crucial role in the formation of carbon-carbon bonds, enabling the synthesis of a wide range of organic compounds, including pharmaceuticals, agrochemicals, and advanced materials.
Used in Catalysis:
4,4,5,5-Tetramethyl-2-(4-methylcyclohex-1-enyl)-1,3,2-dioxaborolane is also utilized in catalysis, where it can act as a catalyst or a catalyst precursor. Its ability to participate in various catalytic cycles makes it a valuable tool for enhancing the efficiency and selectivity of chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,4,5,5-Tetramethyl-2-(4-methylcyclohex-1-enyl)-1,3,2-dioxaborolane is used as a key intermediate in the synthesis of various drug molecules. Its versatility in organic reactions allows for the efficient production of complex pharmaceutical compounds with potential therapeutic applications.
Used in Materials Science:
4,4,5,5-Tetramethyl-2-(4-methylcyclohex-1-enyl)-1,3,2-dioxaborolane is employed in materials science for the synthesis of advanced materials with unique properties. Its ability to form carbon-carbon bonds and participate in various organic reactions contributes to the development of novel materials with potential applications in various fields, such as electronics, energy storage, and nanotechnology.

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  • 4,4,5,5-TETRAMETHYL-2-(4-METHYLCYCLOHEX-1-EN-1-YL)-1,3,2-DIOXABOROLANE

    Cas No: 865869-26-7

  • USD $ 1.9-2.9 / Gram

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  • 865869-26-7 Structure

  • Basic information

    1. Product Name: 4,4,5,5-TETRAMETHYL-2-(4-METHYLCYCLOHEX-1-ENYL)-1,3,2-DIOXABOROLANE
    2. Synonyms: 4,4,5,5-TETRAMETHYL-2-(4-METHYLCYCLOHEX-1-ENYL)-1,3,2-DIOXABOROLANE;4,4,5,5-Tetramethyl-2-(4-methylcyclohex-1-enyl)-1,3,2-dioxaborolane (DDU to USA;1,3,2-Dioxaborolane, 4,4,5,5-tetraMethyl-2-(4-Methyl-1-cyclohexen-1-yl)-;4,4,5,5-TetraMethyl-2-(4-Methyl-1-cyclohexen-1-yl)-1,3,2-dioxaborolane;4,4,5,5-TetraMethyl-2-(4-Methylcyclohex-1-en-1-yl)-1,3,2-dioxaborolane;4-Methyl-1-cyclohexene-1-boronic acid pinacol ester;4-Methyl-1-cyclohexen-1-ylboronic acid pinacol ester;4-Methylcyclohexene-1-boronic Acid Pinacol Ester
    3. CAS NO:865869-26-7
    4. Molecular Formula: C13H23BO2
    5. Molecular Weight: 222.14
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 865869-26-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 245.578oC at 760 mmHg
    3. Flash Point: 102.322oC
    4. Appearance: /
    5. Density: 0.946g/cm3
    6. Vapor Pressure: 0.045mmHg at 25°C
    7. Refractive Index: 1.464
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 4,4,5,5-TETRAMETHYL-2-(4-METHYLCYCLOHEX-1-ENYL)-1,3,2-DIOXABOROLANE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4,4,5,5-TETRAMETHYL-2-(4-METHYLCYCLOHEX-1-ENYL)-1,3,2-DIOXABOROLANE(865869-26-7)
    12. EPA Substance Registry System: 4,4,5,5-TETRAMETHYL-2-(4-METHYLCYCLOHEX-1-ENYL)-1,3,2-DIOXABOROLANE(865869-26-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 865869-26-7(Hazardous Substances Data)

865869-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 865869-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,8,6 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 865869-26:
(8*8)+(7*6)+(6*5)+(5*8)+(4*6)+(3*9)+(2*2)+(1*6)=237
237 % 10 = 7
So 865869-26-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H23BO2/c1-10-6-8-11(9-7-10)14-15-12(2,3)13(4,5)16-14/h8,10H,6-7,9H2,1-5H3

865869-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,5,5-tetramethyl-2-(4-methylcyclohexen-1-yl)-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 4-methyl-1-cyclohexen-1-ylboronic acid pinacol ester

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:865869-26-7 SDS

865869-26-7Relevant articles and documents

Copper-catalyzed cross-coupling of vinyliodonium salts and diboron reagents to generate alkenyl boronic esters

Bao, Robert Li-Yuan,Gan, Shaoyan,Shi, Lei,Zhu, Dan

supporting information, p. 5567 - 5570 (2020/08/21)

An efficient approach for the synthesis of alkenyl boronic esters through the copper-catalyzed cross-coupling of vinyliodonium salts and diboron reagents is reported. This method is distinguished by its mild conditions and short reaction time of less than

INHIBITORS OF HEPATITIS C VIRUS POLYMERASE

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, (2012/06/30)

The present invention provides, among other things, compounds represented by the general Formula (I) and pharmaceutically acceptable salts thereof, wherein X, Y, R1A, R1B, R2, and R3 are as defined in classes and subclasses herein and compositions (e.g., pharmaceutical compositions) comprising such compounds, which compounds are useful as inhibitors of hepatitis C virus polymerase, and thus are useful, for example, as medicaments for the treatment of HCV infection.

QUINAZOLINONE DERIVATIVES AS VIRAL POLYMERASE INHIBITORS

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, (2011/04/19)

Compounds of formula I: (I) wherein X, R2, R3, R5 and R6 are defined herein, are useful as inhibitors of the hepatitis C virus NS5B polymerase.

SUBSTITUTED FUROPYRIMIDINES AND USE THEREOF

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Page/Page column 27, (2011/07/29)

The present application relates to novel substituted furopyrimidine derivatives, to processes for their preparation, to their use for the treatment and/or prophylaxis of diseases and to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, especially for the treatment and/or prophylaxis of cardiovascular diseases.

4-CARBOX PYRAZOLE DERIVATES USEFUL AS ANTI-VIRAL AGENTS

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Page/Page column 65, (2010/02/14)

Novel antiviral compounds of Formula (I) : wherein: A represents hydroxy; R1 represents aryl, heteroaryl bonded through a ring carbon atom, or heterocyclyl bonded through a ring carbon atom, C1-6alkyl or -C5-9cycloalkyl, each of which may be optionally su

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