Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2-(6-METHYL-1-BENZOFURAN-3-YL) ACETIC ACID is a chemical compound with the formula C12H12O3, which is a derivative of benzofuran, an organic compound that contains a benzene ring fused to a furan ring. It is an acetic acid derivative, meaning it contains a carboxylic acid functional group. The presence of the methyl group in the benzofuran ring gives this compound its specific chemical and biological properties, making it useful for various applications.

142917-39-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 142917-39-3 Structure
  • Basic information

    1. Product Name: 2-(6-METHYL-1-BENZOFURAN-3-YL) ACETIC ACID
    2. Synonyms: 2-(6-METHYL-1-BENZOFURAN-3-YL) ACETIC ACID;(6-methyl-1-benzofuran-3-yl)acetic acid(SALTDATA: FREE)
    3. CAS NO:142917-39-3
    4. Molecular Formula: C11H10O3
    5. Molecular Weight: 190.1953
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142917-39-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 344.8°Cat760mmHg
    3. Flash Point: 162.3°C
    4. Appearance: /
    5. Density: 1.267g/cm3
    6. Vapor Pressure: 2.44E-05mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(6-METHYL-1-BENZOFURAN-3-YL) ACETIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(6-METHYL-1-BENZOFURAN-3-YL) ACETIC ACID(142917-39-3)
    12. EPA Substance Registry System: 2-(6-METHYL-1-BENZOFURAN-3-YL) ACETIC ACID(142917-39-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 142917-39-3(Hazardous Substances Data)

142917-39-3 Usage

Uses

Used in Pharmaceutical Industry:
2-(6-METHYL-1-BENZOFURAN-3-YL) ACETIC ACID is used as an intermediate in the synthesis of various drugs and pharmaceutical compounds. Its unique chemical structure allows it to be a valuable building block for the development of new medications.
Used in Research:
2-(6-METHYL-1-BENZOFURAN-3-YL) ACETIC ACID is also used in research as a starting material for the synthesis of more complex organic molecules. Its specific chemical and biological properties make it a promising candidate for the development of novel compounds with potential applications in various fields.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(6-METHYL-1-BENZOFURAN-3-YL) ACETIC ACID is used as a building block for the synthesis of more complex organic molecules. Its unique structure and functional groups make it a versatile component in the creation of new chemical entities with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 142917-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,9,1 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 142917-39:
(8*1)+(7*4)+(6*2)+(5*9)+(4*1)+(3*7)+(2*3)+(1*9)=133
133 % 10 = 3
So 142917-39-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O3/c1-7-2-3-9-8(5-11(12)13)6-14-10(9)4-7/h2-4,6H,5H2,1H3,(H,12,13)/p-1

142917-39-3SDS

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 2-(6-methyl-1-benzofuran-3-yl)acetate

1.2 Other means of identification

Product number -
Other names 6-methylbenzo[b]furan-3-acetic 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:142917-39-3 SDS

142917-39-3Relevant articles and documents

Synthesis and preliminary evaluation of benzofuran-oxadiazole conjugates as potential antitubercular agents

Negalurmath, Veerabhadrayya S.,Kotresh, Obelannavar,Basanagouda, Mahantesha

, p. 965 - 970 (2019/03/07)

In the present study, a series of benzofuran-oxadiazole conjugates 7(a-o) was designed, synthesized and characterized through IR,1H NMR,13C NMR and mass spectral data. All the compounds were screened for preliminary antitubercular activity against Mycobacterium phlei and Mycobacterium tuberculosis H37RV. Among all the target compounds, the compound possessing chlorine (7k, MIC 1.56 μg/mL) and bromine (7m, MIC 1.56 μg/mL) on 6th position of benzofuran showed highest activity against Mycobacterium phlei. Whereas, bromine on either 5th position (7l, MIC 3.125 μg/mL) or 6th position (7m MIC 3.125 μg/mL) on benzofuran exhibited highest activity for Mycobacterium tuberculosis (H37 RV).

Synthesis, anti-microbial and anti-cancer evaluation study of 3-(3-benzofuranyl)-coumarin derivatives

Chougala, Bahubali M.,Shastri, Samundeeswari L.,Holiyachi, Megharaja,Shastri, Lokesh A.,More, Sunil S.,Ramesh

, p. 4128 - 4138 (2015/11/02)

The series of 3-coumarin-substituted benzofuran derivatives 4a-4j have been synthesized under optimized experimental condition with excellent yields. All the isolated compounds were characterized and screened anti-microbiological and anti-cancer activity. The anti-microbiological results observed were extremely good against S. aureus, C. albicans and A. Niger. The comparative docking studies with gyrase type IIA topoisomerase from mycobacterium tuberculosis docked with ligands and 4j have found lowest docked energy.

Efficient and Convenient Method for Synthesis of Benzofuran-3-acetic Acids and Naphthafuran-acetic Acids

Basanagouda, Mahantesha,Narayanachar,Majati, Iranna B.,Mulimani, Shiddappa S.,Sunnal, Satish B.,Nadiger, Rohit V.,Ghanti, Ashok S.,Gudageri, Siddeshwar F.,Naik, Ravi,Nayak, Akshata

supporting information, p. 2195 - 2202 (2015/09/22)

Herein, we report an efficient and convenient method for synthesis of benzofuran-3-acetic acids and naphthafuran-acetic acids 5a-p by the reaction of substituted-4-bromomethylcoumarins with aqueous sodium hydroxide at refluxing temperature. The obtained products are characterized by infrared, 1H NMR, 13C NMR, and mass spectral data. Structures 5a and 5e are confirmed by their single x-ray diffraction studies. The advantages of this method are good yields, easy workup, and no chromatographic purifications.

A convenient synthesis of benzofuran-3-carboxyaldehydes

Deshpande, A. R.,Paradkar, M. V.

, p. 526 - 528 (2007/10/02)

The benzofuran-3-acetic acids (3a-c) on treatment with pyridine N-oxide give benzofuran-3-carboxyaldehydes (5a-c) on reduction with NaBH4 in methanol yields naturally occurring benzofuran 6a which is converted into 6b and 6c by the literature method.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 142917-39-3