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4-((2-Furanmethyl)thio)-2-pentanone, a thioether derivative of 2-pentanone with a furan group attached to the sulfur atom, is a chemical compound characterized by its molecular formula C10H14OS. It is known for its distinctive fruity, nutty aroma and sweet, woody scent, making it a versatile compound in various industries.

180031-78-1

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  • 4-[(2-Furanmethyl)thio]-2-pentanone(4-Furfurylthio-2-pentanone)

    Cas No: 180031-78-1

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180031-78-1 Usage

Uses

Used in the Food Industry:
4-((2-Furanmethyl)thio)-2-pentanone is used as a flavoring agent for its fruity, nutty aroma, enhancing the taste and smell of various food products.
Used in the Fragrance Industry:
In the fragrance industry, 4-((2-Furanmethyl)thio)-2-pentanone is used as a scent component to add a sweet and woody note to perfumes and other scented products, contributing to their unique and appealing olfactory profiles.
Used in Organic Synthesis:
4-((2-Furanmethyl)thio)-2-pentanone also serves as a building block in organic synthesis, utilized for the preparation of various other compounds, showcasing its importance in the realm of chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 180031-78-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,0,3 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 180031-78:
(8*1)+(7*8)+(6*0)+(5*0)+(4*3)+(3*1)+(2*7)+(1*8)=101
101 % 10 = 1
So 180031-78-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O2S/c1-8(11)6-9(2)13-7-10-4-3-5-12-10/h3-5,9H,6-7H2,1-2H3

180031-78-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(furan-2-ylmethylsulfanyl)pentan-2-one

1.2 Other means of identification

Product number -
Other names 4-Furfurylthio-2-pentanone

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:180031-78-1 SDS

180031-78-1Downstream Products

180031-78-1Relevant articles and documents

4-furfurylthiopentanone-2 preparation method

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Paragraph 0039-0040; 0047-0050; 0057-0060; 0067-0070, (2019/11/04)

The invention belongs to the technical field of fine chemistry, and provides a 4-furfurylthiopentanone-2 preparation method, which specifically comprises: adding a raw material chloroacetone to a toluene solution of triphenylphosphine or to triethyl phosphite, and carrying out a heating reflux reaction to obtain a phosphorus salt; dissolving the obtained phosphorus salt in an organic solvent, adding a strong alkali, stirring for 2-3 h, and obtaining phosphorus ylide after completing a reaction; adding the phosphorus ylide to an acetaldehyde aqueous solution or paraldehyde, and stirring until the reaction is completed to obtain 3-pentene-2-ketone; adding piperidine to the 3-pentene-2-ketone, adding a dichloromethane solution of furfuryl mercaptan in a dropwise manner, and controlling the temperature of the system during the adding at 35-40 DEG C; and after the adding, stirring until the reaction is completed so as to obtain the product 4-furfurylthiopentanone-2. According to the present invention, with the method, the problems of high risk, high cost and being unsuitable for industrial production of the 4-furfurylthiopentanone-2 synthesis route in the prior art are solved.

Furfurylthioalkanes, a process for their preparation and their use

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, (2008/06/13)

The invention relates to new furfurylthioalkanes of the formula wherein n can be zero or 1 R represents the methyl or ethyl radical if n is 0, and represents hydrogen or the methyl radical if n is 1, and R' represents methyl or ethyl, a process for their preparation and their use as aroma substances.

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