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3,3,4,4,5,5,5-Heptafluoropentanal, also known as perfluoropentanal, is a halogenated aldehyde with the molecular formula C5F7CHO. It is a colorless liquid characterized by a strong odor. This chemical compound is recognized for its high chemical stability and inertness, which makes it a valuable reagent in organic synthesis. However, due to its potential toxic and irritating effects on the skin, eyes, and respiratory system, it requires careful handling.

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  • 126015-32-5 Structure
  • Basic information

    1. Product Name: 3,3,4,4,5,5,5-HEPTAFLUOROPENTANAL
    2. Synonyms: 3,3,4,4,5,5,5-HEPTAFLUOROPENTANAL
    3. CAS NO:126015-32-5
    4. Molecular Formula: C5H3F7O
    5. Molecular Weight: 212.07
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126015-32-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 89-90°C
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.445±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. Sensitive: Air Sensitive
    10. CAS DataBase Reference: 3,3,4,4,5,5,5-HEPTAFLUOROPENTANAL(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3,3,4,4,5,5,5-HEPTAFLUOROPENTANAL(126015-32-5)
    12. EPA Substance Registry System: 3,3,4,4,5,5,5-HEPTAFLUOROPENTANAL(126015-32-5)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 126015-32-5(Hazardous Substances Data)

126015-32-5 Usage

Uses

Used in Pharmaceutical Industry:
3,3,4,4,5,5,5-Heptafluoropentanal is used as a building block in the synthesis of other fluorinated compounds for the pharmaceutical industry. Its unique properties contribute to the development of new drugs with enhanced efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 3,3,4,4,5,5,5-Heptafluoropentanal serves as a key intermediate in the production of various agrochemicals. Its incorporation into these products can improve their performance and selectivity in agricultural applications.
Used in Organic Synthesis:
3,3,4,4,5,5,5-Heptafluoropentanal is utilized as a valuable reagent in organic synthesis due to its high chemical stability and inertness. This allows for the creation of a wide range of fluorinated compounds with specific properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 126015-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,1 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126015-32:
(8*1)+(7*2)+(6*6)+(5*0)+(4*1)+(3*5)+(2*3)+(1*2)=85
85 % 10 = 5
So 126015-32-5 is a valid CAS Registry Number.

126015-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,4,4,5,5,5-HEPTAFLUOROPENTANAL

1.2 Other means of identification

Product number -
Other names PC5433

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:126015-32-5 SDS

126015-32-5Downstream Products

126015-32-5Relevant articles and documents

β-PERFLUOROALKYLVINYL ALKYL ETHERS

Pazenok, S. V.,Chaika, E. A.,Gerus, I. I.,Yagupol'skii, L. M.

, p. 1238 - 1241 (2007/10/02)

A convenient method was developed for the synthesis of β-perfluoroalkyl-substituted vinyl ethers by the reaction of vinyl alkyl ethers with perfluoroalkyl iodides in the presence of a palladium catalyst.Fluorine-containing aldehydes and their acetals, in which the perfluoroalkyl radical is separated from the formyl group by a methylene unit, were synthesized from the ethers.These aldehydes can be used for the synthesis of β-perfluoroalkyldicarbocyanines.

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