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CAS

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1431330-19-6

[3-bromo-2-(methoxymethoxy)phenyl]boronic acid is a chemical compound that features a boronic acid functional group attached to a phenyl ring, with a bromine atom and a methoxymethoxy group as substituents. [3-bromo-2-(methoxymethoxy)phenyl]boronic acid is known for its potential applications in organic synthesis and medicinal chemistry, particularly in the development of biologically active molecules and pharmaceuticals.

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  • 1431330-19-6 Structure

  • Basic information

    1. Product Name: [3-bromo-2-(methoxymethoxy)phenyl]boronic acid
    2. Synonyms: [3-bromo-2-(methoxymethoxy)phenyl]boronic acid
    3. CAS NO:1431330-19-6
    4. Molecular Formula:
    5. Molecular Weight: 260.88
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1431330-19-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: [3-bromo-2-(methoxymethoxy)phenyl]boronic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: [3-bromo-2-(methoxymethoxy)phenyl]boronic acid(1431330-19-6)
    11. EPA Substance Registry System: [3-bromo-2-(methoxymethoxy)phenyl]boronic acid(1431330-19-6)

  • 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: 1431330-19-6(Hazardous Substances Data)

1431330-19-6 Usage

Uses

Used in Organic Synthesis:
[3-bromo-2-(methoxymethoxy)phenyl]boronic acid is used as a building block for the creation of complex molecules and biologically active compounds. Its boronic acid moiety enables the formation of stable covalent bonds with cis-diol groups, making it a valuable tool in the synthesis of intricate molecular structures.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [3-bromo-2-(methoxymethoxy)phenyl]boronic acid is utilized as a key component in the development of pharmaceuticals. Its ability to form stable bonds with specific molecular groups allows for the creation of novel drugs with targeted therapeutic effects.
Used in Cancer Therapy Development:
[3-bromo-2-(methoxymethoxy)phenyl]boronic acid is used as a potential tool for the development of novel cancer therapies. Its capacity to inhibit proteasome function makes it a promising candidate for the treatment of various types of cancer.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
[3-bromo-2-(methoxymethoxy)phenyl]boronic acid is also employed as a reagent in Suzuki-Miyaura cross-coupling reactions, which are widely used in organic synthesis to form carbon-carbon bonds. The versatility of this reaction, along with the unique properties of [3-bromo-2-(methoxymethoxy)phenyl]boronic acid, makes it an essential component in the synthesis of a wide range of organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1431330-19-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,1,3,3 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1431330-19:
(9*1)+(8*4)+(7*3)+(6*1)+(5*3)+(4*3)+(3*0)+(2*1)+(1*9)=106
106 % 10 = 6
So 1431330-19-6 is a valid CAS Registry Number.

1431330-19-6Relevant articles and documents

Organic compound, and organic light emitting diode and organic light emitting device including the organic compound

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Paragraph 0183; 0188-0191, (2021/05/12)

The present disclosure relates to an organic compound having the following structure, and an organic light emitting diode (OLED) and an organic light emitting device including the organic compound. The organic compound is applied into an emission layer so that the OLED and the organic light emitting device lower their driving voltage, and improves their luminous efficiency and color purity.

Pyrene derivatives comprising heteroaryl amine groupand organic light-emitting diode including the same

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Paragraph 0279-0284, (2016/10/10)

The present invention relates to a pyrene derivative represented by chemical formula A, and an organic light emitting device including the same. In the chemical formula A, a substituent Z, Ar1 to Ar4, and m are the same as described in the specification.COPYRIGHT KIPO 2016

Generation of 3-borylbenzynes, their regioselective Diels-Alder reactions, and theoretical analysis

Takagi, Akira,Ikawa, Takashi,Kurita, Yurio,Saito, Kozumo,Azechi, Kenji,Egi, Masahiro,Itoh, Yuji,Tokiwa, Hiroaki,Kita, Yasuyuki,Akai, Shuji

supporting information, p. 4338 - 4352 (2013/06/04)

3-Borylbenzynes were generated in situ from 6-boryl-2-iodophenyl trifluoromethanesulfonates using i-PrMgCl·LiCl and applied to Diels-Alder reactions with substituted furans and pyrroles. The reactions allowed good functional group compatibility and produced the cycloadducts in high yields with high distal selectivities. Effective conversion of the boryl group of the products was achieved. A series of these reactions provides a new method for producing multifunctionalized benzo-fused aromatic compounds. Additionally, the regioselectivities of these Diels-Alder reactions were theoretically analyzed by DFT calculations to find that the reactions were mainly controlled by the electrostatic effect and aryne distortion caused by the boryl group.

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