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Ethyl 2,2-difluorobutanoate is a colorless liquid chemical compound with the formula C6H10F2O2, characterized by a fruity odor. It is known for its versatility in industrial applications, particularly as a flavoring agent in the food and beverage industry and as an intermediate in the synthesis of pharmaceuticals and agrochemicals.

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  • 2368-92-5 Structure
  • Basic information

    1. Product Name: Ethyl 2,2-difluorobutanoate
    2. Synonyms: Ethyl 2,2-difluorobutanoate;2,2-Difluorobutanoic acid ethyl ester
    3. CAS NO:2368-92-5
    4. Molecular Formula: C6H10F2O2
    5. Molecular Weight: 152.1392064
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2368-92-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 124℃
    3. Flash Point: 29℃
    4. Appearance: /
    5. Density: 1.071
    6. Refractive Index: 1.3665
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ethyl 2,2-difluorobutanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethyl 2,2-difluorobutanoate(2368-92-5)
    11. EPA Substance Registry System: Ethyl 2,2-difluorobutanoate(2368-92-5)
  • 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: 2368-92-5(Hazardous Substances Data)

2368-92-5 Usage

Uses

Used in Food and Beverage Industry:
Ethyl 2,2-difluorobutanoate is used as a flavoring agent to impart a fruity aroma and taste to various food and beverage products, enhancing their overall sensory appeal.
Used in Pharmaceutical Industry:
Ethyl 2,2-difluorobutanoate is used as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Agrochemical Industry:
Ethyl 2,2-difluorobutanoate is also utilized as an intermediate in the production of agrochemicals, playing a role in the development of agricultural products such as pesticides and fertilizers.
Safety Precautions:
Due to its flammable nature, it is crucial to handle Ethyl 2,2-difluorobutanoate with care and follow proper safety measures. Exposure to high concentrations may cause irritation to the respiratory system and skin, necessitating the adoption of appropriate protective measures during its use and storage.

Check Digit Verification of cas no

The CAS Registry Mumber 2368-92-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2368-92:
(6*2)+(5*3)+(4*6)+(3*8)+(2*9)+(1*2)=95
95 % 10 = 5
So 2368-92-5 is a valid CAS Registry Number.

2368-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2,2-difluorobutanoate

1.2 Other means of identification

Product number -
Other names 2,2-Difluor-buttersaeure-aethylester

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:2368-92-5 SDS

2368-92-5Relevant articles and documents

Silver-catalyzed decarboxylative radical allylation of α,α-difluoroarylacetic acids for the construction of CF2-allyl bonds

Wang, Pingyang,Du, Pengcheng,Sun, Qianqian,Zhang, Jianhua,Deng, Hongmei,Jiang, Haizhen

supporting information, p. 2023 - 2029 (2021/03/16)

An efficient silver-catalyzed method of decarboxylative radical allylation of α,α-difluoroarylacetic acids to build CF2-allyl bonds has been developed. Using allylsulfone as an allyl donor, α,α-difluorine substituted arylacetic acids bearing various functional groups are successfully allylated to access a series of 3-(α,α-difluorobenzyl)-1-propylene compounds in moderate to excellent yields in aqueous CH3CN solution under the mild conditions. Experimental studies disclosed that the α-fluorine substitution of arylacetic acid has a great influence on free radical activity and reactivity.

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