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Perfluoro-2,5-dimethyl-3,6-dioxanonanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13252-14-7

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13252-14-7 Usage

Chemical Properties

colorless to clear liquid

Hazard

Moderately toxic by inhalation and skin contact. A moderate eye irritant

Check Digit Verification of cas no

The CAS Registry Mumber 13252-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,5 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13252-14:
(7*1)+(6*3)+(5*2)+(4*5)+(3*2)+(2*1)+(1*4)=67
67 % 10 = 7
So 13252-14-7 is a valid CAS Registry Number.
InChI:InChI=1/C9HF17O4/c10-2(1(27)28,5(14,15)16)29-9(25,26)4(13,7(20,21)22)30-8(23,24)3(11,12)6(17,18)19/h(H,27,28)

13252-14-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,3,3-Tetrafluoro-2-(1,1,2,3,3,3-hexafluoro-2-(perfluoropropoxy)propoxy)propanoic acid

1.2 Other means of identification

Product number -
Other names 2,3,3,3-tetrafluoro-2-[1,1,2,3,3,3-hexafluoro-2-(1,1,2,2,3,3,3-heptafluoropropoxy)propoxy]propanoic acid

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:13252-14-7 SDS

13252-14-7Relevant academic research and scientific papers

2,4,4,5,7,7,8,8,9,9,9-Undecafluoro-2,5-bis(trifluoromethyl)-3, 6-dioxanonyl methacrylate

Paleta, Old?ich,Pale?ek, Ji?í,Michálek, Ji?í

, p. 51 - 53 (2002)

The title monomer (4) was prepared from the trimer of hexafluoropropene-1,2-oxide, 2,4,4,5,7,7,8,8,9,9,9-undecafluoro-2,5-bis(trifluoromethyl)- 3,6-dioxanonanoyl fluoride (1), via methyl ester 2 that was reduced by sodium borohydride to the corresponding alkanol 3, which was finally acylated by methacryloyl chloride.

Synthesis of novel perfluoroalkyl ether derivatives

Shi, Xiang,Shi, Hongxin,Wu, Hongke,Shen, HaiMin

, p. 5091 - 5105 (2018/04/05)

A series of novel fluoroether-containing monomers has been designed and prepared based on the commercially available perfluoroalkyl ether acid fluoride. Treating acid fluoride with allyl alcohol, 2-hydroxyethyl methacrylate or N-allylmethylamine allowed for the direct formation of corresponding vinyl-containing fluorinated monomers. High yields of the fluorinated epoxy monomers could be obtained from acid chloride with glycidol; meanwhile, fluorinated diol was prepared from diethanolamine or 3-amino-1,2-propanediol. Moreover, fluorinated monoamine, fluorinated monoalcohol and fluorinated dichloride were also obtained. Most of these fluorinated monomers were liquid at room temperature and exhibited good solubility in common organic solvents.

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