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4-(4'-Propoxyphenyl)phenylboronic acid is an organic compound characterized by the presence of a boron atom bonded to a phenyl group and a propoxyphenyl group. This unique structure endows it with versatile chemical properties, making it a valuable intermediate in organic synthesis and a potential candidate for various applications in different industries.

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  • 849062-20-0 Structure
  • Basic information

    1. Product Name: 4-(4'-PROPOXYPHENYL)PHENYLBORONIC ACID
    2. Synonyms: 4'-n-Propoxybiphenyl-4-boronic acid, 97%
    3. CAS NO:849062-20-0
    4. Molecular Formula: C15H17BO3
    5. Molecular Weight: 256.1
    6. EINECS: N/A
    7. Product Categories: blocks;BoronicAcids;Aryl;Boronic Acids;Boronic Acids and Derivatives
    8. Mol File: 849062-20-0.mol
  • Chemical Properties

    1. Melting Point: 235-240 °C(lit.)
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /Solid
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(4'-PROPOXYPHENYL)PHENYLBORONIC ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4'-PROPOXYPHENYL)PHENYLBORONIC ACID(849062-20-0)
    11. EPA Substance Registry System: 4-(4'-PROPOXYPHENYL)PHENYLBORONIC ACID(849062-20-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 849062-20-0(Hazardous Substances Data)

849062-20-0 Usage

Uses

Used in Chemical Synthesis:
4-(4'-Propoxyphenyl)phenylboronic acid is used as a reactant in the synthesis of 4''-alkoxy-1,1'':4'',1''-terphenyl-4-carboxylic acids. Its boronic acid functionality allows it to participate in various organic reactions, such as Suzuki-Miyaura cross-coupling, which is a widely used method for the formation of carbon-carbon bonds. This makes it a valuable building block for the preparation of complex organic molecules and pharmaceutical compounds.
Used in Pharmaceutical Industry:
Due to its ability to form stable carbon-carbon bonds, 4-(4'-Propoxyphenyl)phenylboronic acid can be employed as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure may also contribute to the development of new drugs with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Material Science:
The versatile chemical properties of 4-(4'-Propoxyphenyl)phenylboronic acid make it a potential candidate for the development of new materials with specific properties. For example, it can be used in the synthesis of organic semiconductors, which are essential components in electronic devices such as solar cells, light-emitting diodes, and field-effect transistors.
Used in Research and Development:
4-(4'-Propoxyphenyl)phenylboronic acid can be utilized as a research tool in various scientific fields, including organic chemistry, medicinal chemistry, and materials science. Its unique structure and reactivity make it an interesting subject for studying new reaction mechanisms, exploring novel synthetic routes, and developing innovative applications.

Check Digit Verification of cas no

The CAS Registry Mumber 849062-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,0,6 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 849062-20:
(8*8)+(7*4)+(6*9)+(5*0)+(4*6)+(3*2)+(2*2)+(1*0)=180
180 % 10 = 0
So 849062-20-0 is a valid CAS Registry Number.

849062-20-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H55999)  4'-n-Propoxybiphenyl-4-boronic acid, 97%   

  • 849062-20-0

  • 250mg

  • 1295.0CNY

  • Detail
  • Alfa Aesar

  • (H55999)  4'-n-Propoxybiphenyl-4-boronic acid, 97%   

  • 849062-20-0

  • 1g

  • 3886.0CNY

  • Detail

849062-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(4-propoxyphenyl)phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names 4-boronic acid-4'-propyloxybiphenyl

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:849062-20-0 SDS

849062-20-0Upstream product

849062-20-0Relevant articles and documents

Total synthesis and structure-activity relationships of new echinocandin-like antifungal cyclolipohexapeptides

Yao, Jianzhong,Liu, Hongming,Zhou, Ting,Chen, Hai,Miao, Zhenyuan,Sheng, Chunquan,Zhang, Wannian

, p. 196 - 208 (2012/07/28)

A series of new echinocandin-like cyclolipohexapeptides were designed and total synthesized via solution phase [3 + 3]-segment coupling strategy with an attempt to improve antifungal activity. The designed compounds showed potent antifungal activities with broad spectrum. In particular, 11 compounds (i.e. 28a-e, 28g, 28i-j, 29a, 29c and 29e) showed better in vitro antifungal activities against Candida albicans or Aspergillus fumigatus than caspofungin. Moreover, the synthesized compounds provided new SAR information for the echinocandins. The findings in this work suggested that the "left" tripeptide segment of cyclolipohexapeptide scaffold might be a hydrophilic structural motif, whereas the "right" lipopeptide segment was preferred as a hydrophobic core. The amino acid component of the cyclolipohexapeptide scaffold could significantly affect the SAR of the side chains.

Synthesis and property of liquid crystalline 4-alkoxyl-4″-cyano-p-terphenyls

Zang, Zhi-Qian,Zhang, Dong,Wan, Xin-Hua,Zhou, Qi-Feng

, p. 145 - 158 (2007/10/03)

The synthesis of some new 4-alkoxyl-4″-cyano-p-terphenyls is described. The preliminary characterization by means of polarized optical microscopy, differential scanning calorimetry and X-ray diffraction shows that all these compounds are thermotropically liquid-crystalline and can form both the nematic and smectic mesophases.

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