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3-(Tetrahydropyran-2-yloxy)phenylboronic acid is a chemical compound categorized under boronic acids, characterized by a phenylboronic acid group linked to a tetrahydropyran-2-yloxy moiety. 3-(Tetrahydropyran-2-yloxy)phenylboronic acid is recognized for its role in organic synthesis and its potential applications in medicinal chemistry.

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  • 1287777-05-2 Structure
  • Basic information

    1. Product Name: 3-(Tetrahydropyran-2-yloxy)phenylboronic acid
    2. Synonyms: 3-THPO-phenylboronic acid;
    3. CAS NO:1287777-05-2
    4. Molecular Formula: C11H15BO4
    5. Molecular Weight: 222.0454
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1287777-05-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 420.9±55.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.21±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: 7.97±0.10(Predicted)
    10. CAS DataBase Reference: 3-(Tetrahydropyran-2-yloxy)phenylboronic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(Tetrahydropyran-2-yloxy)phenylboronic acid(1287777-05-2)
    12. EPA Substance Registry System: 3-(Tetrahydropyran-2-yloxy)phenylboronic acid(1287777-05-2)
  • 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: 1287777-05-2(Hazardous Substances Data)

1287777-05-2 Usage

Uses

Used in Organic Synthesis:
3-(Tetrahydropyran-2-yloxy)phenylboronic acid is utilized as a reagent in the Suzuki-Miyaura coupling reaction, a pivotal method for the creation of carbon-carbon bonds. This reaction is instrumental in constructing complex organic molecules and plays a significant role in the synthesis of various compounds.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 3-(Tetrahydropyran-2-yloxy)phenylboronic acid is employed as a key intermediate in the preparation of a range of pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Production:
3-(Tetrahydropyran-2-yloxy)phenylboronic acid also finds application in the agrochemical sector, where it is used in the synthesis of various agrochemicals. Its role in this industry is crucial for the development of effective crop protection agents and other agricultural products.
Used in Material Science:
3-(Tetrahydropyran-2-yloxy)phenylboronic acid contributes to the advancement of material science by being a component in the synthesis of new materials with specific properties required for various applications.
Used in Cancer Research and Treatment:
3-(Tetrahydropyran-2-yloxy)phenylboronic acid has demonstrated potential anti-cancer activities, making it a valuable compound for research and development in oncology. Its exploration in this field could lead to the discovery of new cancer therapeutics.
Used in Inflammation and Anti-Inflammatory Research:
3-(Tetrahydropyran-2-yloxy)phenylboronic acid's potential anti-inflammatory properties position it as a candidate for research into treatments for inflammatory conditions, offering new avenues for managing such diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 1287777-05-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,7,7,7 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1287777-05:
(9*1)+(8*2)+(7*8)+(6*7)+(5*7)+(4*7)+(3*7)+(2*0)+(1*5)=212
212 % 10 = 2
So 1287777-05-2 is a valid CAS Registry Number.

1287777-05-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-((Tetrahydro-2H-pyran-2-yl)oxy)phenyl)boronic acid

1.2 Other means of identification

Product number -
Other names [3-(oxan-2-yloxy)phenyl]boronic acid

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:1287777-05-2 SDS

1287777-05-2Relevant articles and documents

Synthesis and characterization of achiral bent-core liquid crystalline molecules containing salicylaldimine-based with a wide temperature range of SmCP phase

Liao, Chien-Tung,Liu, Jung-Yo,Zou, Sing-Fang,Wu, Nien-Chieh,Wu, Zheng-Long,Lee, Jiunn-Yih

, p. 124 - 133 (2011/04/15)

The design and synthesis of a series bent-core materials base on a 3,4'-biphenyldiol central core containing salicylaldimine-based and two terminal tetradecyloxy tails are reported. In addition, the effects of lateral substituents (R = F and Cl) at the biphenyl core into 3'-position are examined. These substituents have a strong influence in reducing the clearing temperatures and increasing temperature range of SmCP phase. Upon cooling process the isotropic liquid, compound SB-Cl exhibits the lowest clearing transition temperature of 180 oC and the widest SmCP phase range of 129 °C. The mesophase behaviour were investigated by polarizing optical microscopy (POM), differential scanning calorimetry (DSC), X-ray diffraction (XRD), and electro-optical (EO) measurements in the mesophase temperature range.

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