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Methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate is an organic compound characterized by its complex chemical structure. It belongs to the class of acetate esters and is widely recognized as a versatile building block in organic synthesis. Methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate is known for its mild and adaptable reactivity, making it a valuable asset in the field of organic chemistry.

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  • METHYL 2-(2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL)ACETATE

    Cas No: 956229-86-0

  • USD $ 1.9-2.9 / Gram

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  • 956229-86-0 Structure
  • Basic information

    1. Product Name: Methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate
    2. Synonyms: 2-(Methoxycarbonylmethyl)phenylboronic acid pinacol ester;Methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate;methyl 2-[2-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate;2-(2-Methoxy-2-oxoethyl)benzeneboronicacid,pinacolester96%;Methyl [2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate
    3. CAS NO:956229-86-0
    4. Molecular Formula: C15H21BO4
    5. Molecular Weight: 276.13584
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 956229-86-0.mol
  • Chemical Properties

    1. Melting Point: 66-68 °C
    2. Boiling Point: 371.7±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.07±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: Methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate(956229-86-0)
    11. EPA Substance Registry System: Methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate(956229-86-0)
  • 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: 956229-86-0(Hazardous Substances Data)

956229-86-0 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity enable the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Industry:
In the agrochemical sector, Methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate serves as a crucial component in the production of pesticides and other agrochemicals. Its incorporation into these products enhances their effectiveness in protecting crops and controlling pests.
Used in Perfume and Fragrance Industry:
Methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate is utilized as a raw material in the creation of perfumes and fragrances. Its distinctive chemical properties contribute to the development of unique and complex scents, enriching the olfactory experience.
Used as a Reagent in Chemical Reactions:
Methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate is employed as a reagent in a variety of chemical reactions, including cross-coupling and Suzuki-Miyaura reactions. Its mild reactivity allows for the formation of new chemical bonds with high selectivity and efficiency, facilitating the synthesis of complex organic molecules for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 956229-86-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,2,2 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 956229-86:
(8*9)+(7*5)+(6*6)+(5*2)+(4*2)+(3*9)+(2*8)+(1*6)=210
210 % 10 = 0
So 956229-86-0 is a valid CAS Registry Number.

956229-86-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate

1.2 Other means of identification

Product number -
Other names -

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:956229-86-0 SDS

956229-86-0Relevant articles and documents

LIPOXYGENASE INHIBITORS

-

Paragraph 00609, (2021/07/02)

Various embodiments of the present disclosure are directed to compounds having Formula I, Formula II, Formula IIA, Formula III, Formula IIIA, Formula IIIB, and/or pharmaceutically acceptable salts thereof. The compounds can be suitable for inhibiting lipoxygenases and/or treating associated diseases. In some embodiments, subject compounds are used to prepare a composition that is effective in treating neurodegenerative diseases.

Internal Nucleophilic Catalyst Mediated Cyclisation/Ring Expansion Cascades for the Synthesis of Medium-Sized Lactones and Lactams

Lawer, Aggie,Rossi-Ashton, James A.,Stephens, Thomas C.,Challis, Bradley J.,Epton, Ryan G.,Lynam, Jason M.,Unsworth, William P.

, p. 13942 - 13947 (2019/08/28)

A strategy for the synthesis of medium-sized lactones and lactams from linear precursors is described in which an amine acts as an internal nucleophilic catalyst to facilitate a novel cyclisation/ring expansion cascade sequence. This method obviates the n

TARGETED TREATMENT OF LEIOMYOSARCOMA

-

, (2016/10/31)

A method and medicament comprising 4,4,4-trifluoro-N-[(1S)-2-[[(7S)-5-(2- hydroxyethyl)-6-oxo-7H-pyrido[2,3-d][3]benzazepin-7-yl]amino]-1-methyl-2-oxo- ethyl]butanamide or a pharmaceutically acceptable salt or hydrate thereof for treating leiomyosarcoma i

PHOTOCHROMIC THIENOCHROMENE COMPOUNDS

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Paragraph 0189, (2016/09/26)

The present invention relates to photochromic compounds, such as thienochromene compounds represented by the following Formulas (la) and/or (lb). The present invention also relates to photochromic compositions and articles containing one or more such phot

NOTCH PATHWAY SIGNALING INHIBITOR COMPOUND

-

, (2013/03/26)

The present invention provides a compound, or a pharmaceutically acceptable salt or hydrate, and a pharmaceutical composition containing said compound, or a pharmaceutically acceptable salt or hydrate, useful as a Notch pathway signaling inhibitor for the

One-pot synthesis of new aza- and diaza-aminophenanthrenes

Rochais, Christophe,Yougnia, Rodrigue,Cailly, Thomas,Sopková-De Oliveira Santos, Jana,Rault, Sylvain,Dallemagne, Patrick

experimental part, p. 5806 - 5810 (2011/08/09)

The synthesis of a series of benzo(iso)quinoline and phenanthroline derivatives has been achieved using an efficient one-pot procedure. It proceeds through a Suzuki-Miyaura cross-coupling followed by a Dieckmann-Thorpe ring closure under microwave irradia

One-pot synthesis of novel poly-substituted phenanthrenes

Yougnia, Rodrigue,Rochais, Christophe,Oliveira Santos, Jana Sopkovà-de,Dallemagne, Patrick,Rault, Sylvain

experimental part, p. 2803 - 2808 (2010/06/16)

A one-pot synthesis of novel poly-substituted phenanthrenes is described in this article through a Suzuki-Miyaura cross-coupling followed by a Dieckmann-Thorpe ring closure under microwave irradiation. The selection of the appropriate starting materials allowed us to introduce diversity on various positions of the phenanthrene ring system.

PHENANTHRENE DERIVATIVES AS MPGES-1 INHIBITORS

-

, (2008/06/13)

The invention encompasses novel compounds of Formula or pharmaceutically acceptable salts thereof. These compounds are inhibitors of the microsomal prostaglandin E synthase-1 (mPGES-1) enzyme and are therefore useful to treat pain and/or inflammation from a variety of diseases or conditions, such as osteoarthritis, rheumatoid arthritis and acute or chronic pain. Methods of treating diseases or conditions mediated by the mPGES-1 enzyme and pharmacuetical compositions are also encompassed

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