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1578-56-9

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1578-56-9 Usage

General Description

2-Fluorovaleric acid is a chemical compound with the molecular formula C5H9FO2. It is a colorless liquid that is derived from valeric acid by substituting one of the hydrogen atoms with a fluorine atom. 2-Fluorovaleric acid has various industrial applications, including as a building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. 2-Fluorovaleric acid is also used in the production of flavors and fragrances. It is important to handle this chemical with care, as it can cause irritation to the skin, eyes, and respiratory system upon contact or inhalation.

Check Digit Verification of cas no

The CAS Registry Mumber 1578-56-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1578-56:
(6*1)+(5*5)+(4*7)+(3*8)+(2*5)+(1*6)=99
99 % 10 = 9
So 1578-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H9FO2/c1-2-3-4(6)5(7)8/h4H,2-3H2,1H3,(H,7,8)

1578-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoropentanoic acid

1.2 Other means of identification

Product number -
Other names 2-Fluorovaleric 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:1578-56-9 SDS

1578-56-9Relevant articles and documents

SARTAN ANALOGUE

-

, (2019/07/23)

The invention concerns a sartan analogue on basis of a sartan which sartan comprises an alkyl group or an alkoxy group, wherein the sartan analogue only differs from the sartan by a replacement of the alkyl group or the alkoxy group or replacement of a methyl residue or a hydrogen residue of the alkyl group or of the alkoxy group by a fluorine atom.

Studies of a diastereoselective electrophilic fluorination reaction employing a cryo-flow reactor

Nakayama, Keiji,Browne, Duncan L.,Baxendale, Ian R.,Ley, Steven V.

, p. 1298 - 1302 (2013/07/27)

The application of meso-scale flow chemistry in research laboratories continues to increase. Here, we report on the use of a modular cryo-flow device as applied to a diastereoselective fluorination process. The reactor can be incorporated into existing flow chemistry setups to permit continuous processing at low temperatures without recourse to cryogenic consumables. Georg Thieme Verlag Stuttgart. New York.

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