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2-(Perfluoro-n-hexyl)acetaldehyde dimethyl acetal is a unique chemical compound characterized by the presence of fluorine atoms, where all hydrogen atoms are substituted by fluorine. This perfluorinated compound features an n-hexyl chain, which consists of six carbon atoms, and a dimethyl acetal group, where two methyl groups are attached to an acetal moiety. It serves as a versatile starting material in the synthesis of various chemicals and is utilized in scientific research.

142502-76-9

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142502-76-9 Usage

Uses

Used in Chemical Synthesis:
2-(Perfluoro-n-hexyl)acetaldehyde dimethyl acetal is used as a starting material for the production of a range of chemicals. Its unique structure, with fluorine atoms and an n-hexyl chain, allows for the creation of compounds with specific properties tailored for various applications.
Used in Scientific Research:
In the field of scientific research, 2-(Perfluoro-n-hexyl)acetaldehyde dimethyl acetal is employed as a compound of interest for studying its properties and potential applications. Researchers may investigate its reactivity, stability, and interactions with other molecules, contributing to the broader understanding of perfluorinated compounds and their potential uses in various industries.
Used in Pharmaceutical Industry:
2-(Perfluoro-n-hexyl)acetaldehyde dimethyl acetal may be used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure could potentially contribute to the development of new drugs with improved properties, such as enhanced solubility, bioavailability, or targeted delivery.
Used in Material Science:
In material science, 2-(Perfluoro-n-hexyl)acetaldehyde dimethyl acetal could be utilized in the development of novel materials with specific characteristics, such as improved thermal stability, chemical resistance, or surface properties. Its perfluorinated nature may offer advantages in the creation of materials for specialized applications, such as in aerospace or electronics.

Check Digit Verification of cas no

The CAS Registry Mumber 142502-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,5,0 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 142502-76:
(8*1)+(7*4)+(6*2)+(5*5)+(4*0)+(3*2)+(2*7)+(1*6)=99
99 % 10 = 9
So 142502-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H9F13O2/c1-24-4(25-2)3-5(11,12)6(13,14)7(15,16)8(17,18)9(19,20)10(21,22)23/h4H,3H2,1-2H3

142502-76-9Downstream Products

142502-76-9Relevant academic research and scientific papers

Synthesis of vicinal perfluoroalkyl enol ethers

Zoghlami,Chehidi,Chaabouni,Baklouti

, p. 1887 - 1892 (2007/10/03)

A convenient preparation of vicinal perfluoroalkyl enol ethers, by the action of alcohols on 1-bromo-1-perfluoroalkylethylenes in the presence of potassium hydroxide, is described. Some aspects of their reactivity are reported.

Synthesis of fluoroalkyl ethanal: R(F)CH2CHO

Laurent,Blancou,Commeyras

, p. 2489 - 2492 (2007/10/02)

Aldehydes R(F)CH2CHO (R(F) is a linear perfluoroalkyl chain) have been obtained in the addition reaction of R(F)I to vinyl acetate in the presence of zinc. R(F)CH2CHIOAc is formed as an intermediate in the course of the reaction. Under appropriate conditions, R(F)CH2CHO and its acylal or acetal derivatives are obtained in good yields.

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