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4,4,5-trifluoro-2,5-bis(trifluoromethyl)-1,3-dioxolane-2-carbonyl fluoride is a complex organic compound with the molecular formula C5F8O3. It is characterized by the presence of three fluorine atoms attached to the central carbon atom, two trifluoromethyl groups (CF3) on the adjacent carbon atoms, and a carbonyl fluoride group (COF) attached to the carbonyl carbon. This molecule features a 1,3-dioxolane ring, which is a five-membered cyclic ether with two oxygen atoms. The compound is known for its stability and reactivity, making it a valuable intermediate in the synthesis of various fluorinated compounds. Due to its highly fluorinated nature, it exhibits unique properties such as high electronegativity and lipophilicity, which can be exploited in various chemical reactions and applications.

7385-65-1

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7385-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7385-65-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,8 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7385-65:
(6*7)+(5*3)+(4*8)+(3*5)+(2*6)+(1*5)=121
121 % 10 = 1
So 7385-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C6F10O3/c7-1(17)2(4(9,10)11)18-3(8,5(12,13)14)6(15,16)19-2

7385-65-1SDS

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 4,4,5-trifluoro-2,5-bis(trifluoromethyl)-1,3-dioxolane-2-carbonyl fluoride

1.2 Other means of identification

Product number -
Other names EINECS 230-965-5

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:7385-65-1 SDS

7385-65-1Relevant academic research and scientific papers

FLUOROLACTONE AND METHOD FOR PRODUCING SAME

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Paragraph 0291-0294, (2021/12/03)

The present disclosure provides, for example, a method that can produce a fluorolactone compound from hexafluoropropylene oxide or the like in a single step. The present disclosure relates to a method for producing a compound represented by formula (1): wherein two R1 are the same and each is a fluorine atom or a fluoroalkyl group, the method comprising step A of reacting a compound represented by formula (2): wherein R1 is as defined above, with a compound (3) represented by formula (3-1) or the like: wherein R31, R32, and R33 are the same or different and each is a hydrogen atom or a C1-10 alkyl group, or two of them are optionally linked to each other to form a ring optionally having one or more substituents, in the presence of a fluorine compound (4) represented by formula (4-1) or the like: [in-line-formulae]MHnFm(4-1)[/in-line-formulae] wherein M is a metal atom, n is 0 or 1, and the sum of the valence number of M and n is m, and an organic solvent, provided that the compound represented by formula (3) is excluded from the organic solvent.

METHOD FOR PRODUCING PERFLUORO (2,4-DIMETHYL-2-FLUOROFORMYL-1,3-DIOXOLANE)

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Paragraph 0046-0065, (2020/12/15)

PROBLEM TO BE SOLVED: To provide a production method which can produce a perfluoro (2,4-dimethyl-2-fluoroformyl-1,3-dioxolane) with a good yield while containing a trifluoropyruvic acid fluoride dimer and/or trifluoropyruvic acid fluoride as raw materials. SOLUTION: A method for producing perfluoro (2,4-dimethyl-2-fluoroformyl-1,3-dioxolane) includes: a reaction step of reacting at least one synthesis raw material selected from the group consisting of a trifluoropyruvic acid fluoride dimer and trifluoropyruvic acid fluoride with a hexafluoropropylene oxide in the presence of a fluoride in an organic solvent; a by-product decomposition step of decomposing a by-product in a reaction liquid obtained in the reaction step; and an isomerization step after the by-product decomposition step. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Hexafluoropropylene oxide is added to the aldehyde, and method for producing an α [...] acid (by machine translation)

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Paragraph 0051, (2020/04/09)

[A] producing an α for [...] acid, industrially feasible method. [Solution] the step of reacting an aldehyde with hexafluoropropylene oxide, an α [...] acid production. [Drawing] no (by machine translation)

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