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430-50-2

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430-50-2 Usage

General Description

1-Fluoro-2-propanol is a chemical compound with the molecular formula C3H7FO. It is a colorless liquid with a faint odor and is used in various chemical reactions and processes. 1-FLUORO-2-PROPANOL is primarily used as a solvent in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. It is also used in the production of dyes, coatings, and flavors. 1-Fluoro-2-propanol is considered to have low toxicity, but exposure to high levels of this compound can cause irritation to the eyes, skin, and respiratory system. Additionally, it is important to handle 1-fluoro-2-propanol with caution, as it is highly flammable and should be stored and handled in a well-ventilated area.

Check Digit Verification of cas no

The CAS Registry Mumber 430-50-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 430-50:
(5*4)+(4*3)+(3*0)+(2*5)+(1*0)=42
42 % 10 = 2
So 430-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H7FO/c1-3(5)2-4/h3,5H,2H2,1H3

430-50-2SDS

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 1-fluoropropan-2-ol

1.2 Other means of identification

Product number -
Other names 1-fluoropropane-2-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:430-50-2 SDS

430-50-2Relevant articles and documents

One-way biohydrogen transfer for oxidation of sec-alcohols

Lavandera, Ivan,Kern, Alexander,Resch, Verena,Ferreira-Silva, Bianca,Glieder, Anton,Fabian, Walter M. F.,De Wildeman, Stefaan,Kroutil, Wolfgang

supporting information; experimental part, p. 2155 - 2158 (2009/05/27)

(Chemical Equation Presented) Quasi-irreversible oxidation of sec-alcohols was achieved via biocatalytic hydrogen transfer reactions using alcohol dehydrogenases employing selected ketones as hydrogen acceptors, which can only be reduced but not oxidized. Thus, only 1 equiv of oxidant was required instead of a large excess. For the oxidation of both isomers of methylcarbinols a single nonstereoselective short-chain dehydrogenase/reductase from Sphingobium yanoikuyae was identified and overexpressed in E. coli.

LABELED COCAINE ANALOGS

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, (2008/06/13)

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