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2,3,5-Trimethylfuran, a derivative of furan, is a flammable, colorless liquid characterized by a sweet odor. It is recognized for its high energy content and low environmental impact, making it a promising candidate for various applications across different industries.

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  • 10504-04-8 Structure
  • Basic information

    1. Product Name: 2,3,5-TRIMETHYLFURAN
    2. Synonyms: 2,3,5-TRIMETHYLFURAN;SALOR-INT L159735-1EA
    3. CAS NO:10504-04-8
    4. Molecular Formula: C7H10O
    5. Molecular Weight: 110.15
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10504-04-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 126°Cat760mmHg
    3. Flash Point: 20°C
    4. Appearance: /
    5. Density: 0,89 g/cm3
    6. Vapor Pressure: 14.4mmHg at 25°C
    7. Refractive Index: 1.457
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,3,5-TRIMETHYLFURAN(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3,5-TRIMETHYLFURAN(10504-04-8)
    12. EPA Substance Registry System: 2,3,5-TRIMETHYLFURAN(10504-04-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 11-20/22-36/37/38
    3. Safety Statements: 16-26-36/37/39
    4. RIDADR: 1993
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 10504-04-8(Hazardous Substances Data)

10504-04-8 Usage

Uses

Used in Chemical Synthesis:
2,3,5-Trimethylfuran is used as a solvent in chemical reactions for its ability to dissolve a wide range of substances, facilitating various chemical processes.
Used in Chemical Production:
It serves as an intermediate in the production of other chemicals, contributing to the synthesis of complex organic compounds.
Used in Biofuel Industry:
2,3,5-Trimethylfuran is used as a potential biofuel due to its high energy content and the reduced environmental impact compared to traditional fossil fuels, offering a sustainable energy alternative.
Used in Flavor and Fragrance Industry:
It is utilized as a flavor and fragrance ingredient, capitalizing on its sweet odor to enhance the sensory properties of various products.
Used in Antimicrobial Applications:
2,3,5-Trimethylfuran is explored for its antimicrobial properties, indicating potential use in sanitizing products or as a preservative in different industries to inhibit microbial growth.

Check Digit Verification of cas no

The CAS Registry Mumber 10504-04-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,0 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10504-04:
(7*1)+(6*0)+(5*5)+(4*0)+(3*4)+(2*0)+(1*4)=48
48 % 10 = 8
So 10504-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O/c1-5-4-6(2)8-7(5)3/h4H,1-3H3

10504-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5-TRIMETHYLFURAN

1.2 Other means of identification

Product number -
Other names Furan,2,3,5-trimethyl

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:10504-04-8 SDS

10504-04-8Relevant articles and documents

1H and 13C NMR Spectra of Some 2-Substituted 4,5-Dimethylfurans

Dandarova, Miloslava,Vegh, Daniel

, p. 1141 - 1144 (1992)

1H and 13C NMR spectra of 22 2-substituted 4,5-dimethylfurans are reported.The J(C,H) values were used for signal assignments and for the identification of geometrical isomers of some derivatives. KEY WORDS: 2-Substituted 4,5-dimethylfurans, 1H and 13C NMR spectra

METAL CATALYST AND HYDROGEN GAS FREE APPROACHES FOR SELECTIVE REDUCTION OF ALDEHYDE TO METHYL GROUP OF DIFFERENT SUBSTITUTED FURANS

-

Page/Page column 19, (2021/08/27)

The present invention relates to 5-methyl substituted furan compounds of general formula (I) and process for the preparation thereof: OR1R2 R3CH3(I) Particularly, the present invention relates to a metal catalyst and hydrogen gas free, atom-economy, highly selective and low-cost process for the preparation of methyl substituted furan compounds from different aldehyde substituted furan compounds.

Hydrogen peroxide oxidation of polysubstituted pyrylium salts: Formation of enol esters and furans

Balaban, Teodor Silviu,Hiegemann, Monika

, p. 9827 - 9840 (2007/10/02)

2,4,6-Trialkylsubstituted pyrylium salts 1 have been known to afford 2-acyl-3,5-dialkyl-furans 2 in moderate yields (30 - 45%). Oxidation of these salts in buffer solutions (pH = 3-4.5) increased the yields of acylfurans to 75%. In contrast, tetra- and pe

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