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423-56-3

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423-56-3 Usage

Description

1H,1H-Perfluoro-1-nonanol is a synthetic, perfluorinated organic compound characterized by its unique chemical properties. It is a white transparent crystalline solid with a high degree of fluorination, which contributes to its distinct characteristics and potential applications in various industries.

Uses

1. Used in Chemical Synthesis:
1H,1H-Perfluoro-1-nonanol is used as a key intermediate in the production of other chemicals, particularly those with perfluorinated structures. Its high reactivity and unique properties make it a valuable precursor for synthesizing a range of compounds with specific applications.
2. Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1H,1H-Perfluoro-1-nonanol is used as a starting material for the synthesis of various perfluorinated drugs and drug candidates. Its unique properties, such as high lipophilicity and resistance to metabolic degradation, can be exploited to enhance the pharmacokinetic and pharmacodynamic profiles of these drugs.
3. Used in Material Science:
1H,1H-Perfluoro-1-nonanol can be utilized in the development of novel materials with specific properties, such as low surface energy, chemical resistance, and thermal stability. These materials can find applications in various fields, including coatings, lubricants, and membranes.
4. Used in the Production of Trifluoro-methanesulfonic Acid 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-heptadecafluoro-nonyl Ester:
1H,1H-Perfluoro-1-nonanol is used as a reactant in the synthesis of Trifluoro-methanesulfonic acid 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-heptadecafluoro-nonyl ester. This reaction requires the use of Pyridine as a reagent and CHCl3 (Chloroform) as a solvent, highlighting the versatility of 1H,1H-Perfluoro-1-nonanol in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 423-56-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,2 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 423-56:
(5*4)+(4*2)+(3*3)+(2*5)+(1*6)=53
53 % 10 = 3
So 423-56-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H3F17O/c10-2(11,1-27)3(12,13)4(14,15)5(16,17)6(18,19)7(20,21)8(22,23)9(24,25)26/h27H,1H2

423-56-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Detail
  • TCI America

  • (H1232)  1H,1H-Heptadecafluoro-1-nonanol  >97.0%(GC)

  • 423-56-3

  • 5g

  • 560.00CNY

  • Detail
  • Alfa Aesar

  • (L16600)  1H,1H-Perfluoro-1-nonanol, 98%   

  • 423-56-3

  • 5g

  • 422.0CNY

  • Detail
  • Aldrich

  • (446823)  2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-Heptadecafluoro-1-nonanol  96%

  • 423-56-3

  • 446823-5G

  • 553.41CNY

  • Detail

423-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H,1H-PERFLUORO-1-NONANOL

1.2 Other means of identification

Product number -
Other names 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-heptadecafluorononan-1-ol

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:423-56-3 SDS

423-56-3Upstream product

423-56-3Relevant articles and documents

Thermal desulfurization of (Alkoxymethyl)thiiranes

Nalet'Ko,Pervova,Gorbunova,Zapevalov, A. Ya,Toporova,Saloutin

, p. 2120 - 2124 (2015/02/02)

Reaction of (alkoxymethyl)oxiranes with thiourea in methanol has afforded the corresponding thiiranes, and catalyst-free thermal desulfurization of the products has been studied. The major products of desulfurization are alcohols and alkenes, both in the cases of (polyfluoroalkyloxymethyl)thiiranes and their non-fluorinated analogs. Longer alkyl chain in thiiranes favors formation of alcohols over alkenes formation in the course of desulfurization.

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