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1-BENZOFURAN-3-YLACETALDEHYDE 97, a chemical compound with the molecular formula C11H8O2, is a yellow to brown liquid characterized by a strong, sweet, floral odor. This versatile compound is utilized in various applications, primarily in the synthesis of pharmaceuticals and fragrances, and also serves as a flavoring agent.

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  • 352434-24-3 Structure
  • Basic information

    1. Product Name: 1-BENZOFURAN-3-YLACETALDEHYDE 97
    2. Synonyms: 1-BENZOFURAN-3-YLACETALDEHYDE 97;1-BENZOFURAN-3-YLACETALDEHYDE;BENZO[B]FURAN-3-YLACETALDEHYDE;1-Benzofuran-3-ylacetaldehyde 97%;3-Benzofuranacetaldehyde
    3. CAS NO:352434-24-3
    4. Molecular Formula: C10H8O2
    5. Molecular Weight: 160.16932
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 352434-24-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 272.8 °C at 760 mmHg
    3. Flash Point: 121.9 °C
    4. Appearance: /
    5. Density: 1.173g/cm3
    6. Vapor Pressure: 0.00596mmHg at 25°C
    7. Refractive Index: 1.591
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-BENZOFURAN-3-YLACETALDEHYDE 97(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-BENZOFURAN-3-YLACETALDEHYDE 97(352434-24-3)
    12. EPA Substance Registry System: 1-BENZOFURAN-3-YLACETALDEHYDE 97(352434-24-3)
  • 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: 352434-24-3(Hazardous Substances Data)

352434-24-3 Usage

Uses

Used in Pharmaceutical Industry:
1-BENZOFURAN-3-YLACETALDEHYDE 97 is used as a key intermediate in the synthesis of various pharmaceuticals for its unique chemical properties that contribute to the development of new drugs.
Used in Fragrance Industry:
1-BENZOFURAN-3-YLACETALDEHYDE 97 is used as a fragrance ingredient for its strong, sweet, floral scent, enhancing the aroma profiles of various perfumes and scented products.
Used as a Flavoring Agent:
1-BENZOFURAN-3-YLACETALDEHYDE 97 is used to impart flavor to food and beverages, capitalizing on its distinctive taste and aroma to create unique flavor combinations.
Safety and Storage:
It is crucial to handle 1-BENZOFURAN-3-YLACETALDEHYDE 97 with care due to its potential to cause irritation to the skin, eyes, and respiratory system. To ensure safety, it should be stored in a cool, dry place, away from sources of ignition and incompatible materials.

Check Digit Verification of cas no

The CAS Registry Mumber 352434-24-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,4,3 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 352434-24:
(8*3)+(7*5)+(6*2)+(5*4)+(4*3)+(3*4)+(2*2)+(1*4)=123
123 % 10 = 3
So 352434-24-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O2/c11-6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,6-7H,5H2

352434-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-benzofuran-3-yl)acetaldehyde

1.2 Other means of identification

Product number -
Other names OR8671

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:352434-24-3 SDS

352434-24-3Relevant articles and documents

Asymmetric dearomatic diels-alder reactions of diverse heteroarenes via π-system activation

Xiao, You-Cai,Yue, Cai-Zhen,Chen, Peng-Qiao,Chen, Ying-Chun

supporting information, p. 3208 - 3211 (2014/07/08)

An asymmetric dearomatic Diels-Alder protocol for various heteroarenes, such as benzofuran, benzothiophene, or even furan, has been developed via π-system activation. This method involves in situ generation of formal trienamine species embedding a heteroa

Development of rationally designed DNA N6 adenine methyltransferase inhibitors

Hobley, Gerard,McKelvie, Jennifer C.,Harmer, Jenny E.,Howe, Jason,Oyston, Petra C.F.,Roach, Peter L.

, p. 3079 - 3082 (2012/06/17)

A series of bisubstrate inhibitors for DNA N6 adenine methyltransferase (Dam) have been synthesized by linking an amine analogue of S-adenosylmethionine to an aryl moiety designed to probe the binding pocket of the DNA adenine base. An initial structure-activity relationship study has identified substituents that increase inhibitor potency to the ~10 μM range and improve selectivity against the human cytosine methyltransferase Dnmt1.

INHIBITORS OF THE INTERACTION BETWEEN MDM2 AND P53

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Page/Page column 37, (2008/06/13)

The present invention provides compounds of formula (I), their use as an inhibitor of a p53-MDM2 interaction as well as pharmaceutical compositions comprising said compounds of formula (I) wherein n, m, p, s, t, R1, R2, A and Z have

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