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114810-56-9

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114810-56-9 Usage

General Description

4,5,5,5-TETRAFLUORO-4-TRIFLUOROMETHYL-2-IODOPENTAN-1-OL is a chemical compound with the molecular formula C7H5F7IO. It is a fluorinated compound with a trifluoromethyl group and an iodine atom attached to a pentanol chain. 4,5,5,5-TETRAFLUORO-4-TRIFLUOROMETHYL-2-IODOPENTAN-1-OL is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It is also used as a reagent in organic chemistry for the introduction of fluorine and iodine atoms into organic molecules. Due to its unique structure and properties, 4,5,5,5-TETRAFLUORO-4-TRIFLUOROMETHYL-2-IODOPENTAN-1-OL has a wide range of applications in research and industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 114810-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,8,1 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 114810-56:
(8*1)+(7*1)+(6*4)+(5*8)+(4*1)+(3*0)+(2*5)+(1*6)=99
99 % 10 = 9
So 114810-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H6F7IO/c7-4(5(8,9)10,6(11,12)13)1-3(14)2-15/h3,15H,1-2H2

114810-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5,5,5-tetrafluoro-2-iodo-4-(trifluoromethyl)pentan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:114810-56-9 SDS

114810-56-9Downstream Products

114810-56-9Relevant articles and documents

Fluorinated epoxides 6. Chemoselectivity in the preparation of 2-[(heptafluoroisopropyl)methyl]oxirane from iodoacetate and iodohydrin precursors

Církva, Vladimír,Duchek, Jan,Paleta, Old?ich

, p. 101 - 104 (2007/10/03)

Fluorinated iodoacetate (CF3)2CFCH2 CHICH2OAc (1) (prepared by radical addition of perfluoroisopropyl iodide to allyl acetate) and fluorinated iodohydrin (CF3)2CFCH2CHICH2OH (2) (prepared from 1) were converted to the corresponding perfluoroalkylated oxirane (CF3)2CFCH2CH(-O-)CH2 (3) in the yield of 62%. The chemoselectivity of the oxirane formation appeared to be strongly dependent on the starting compound 1 or 2 and solvent used. Byproducts (CF3)2CFCH= CHCH2OH (4) and (CF3)2CFCH= CHCH2OAc (5) can form a major part of the products in the formation of epoxide 3.

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