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1-Butanol, 3-chloro-, also known as 3-chloro-1-butanol or chlorobutanol, is an organic compound with the chemical formula C4H9ClO. It is a colorless, oily liquid with a mild, chloroform-like odor. 1-Butanol, 3-chloro- is primarily used as a preservative in various pharmaceutical and cosmetic products due to its ability to inhibit the growth of bacteria, fungi, and other microorganisms. It is also employed as a solvent in the synthesis of other chemicals and as a stabilizer in the production of certain polymers. However, its use has been restricted in some applications due to potential health concerns and the development of alternative preservatives.

2203-35-2

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2203-35-2 Usage

Synonyms

Chloroisoamyl alcohol

Physical State

Colorless liquid

Odor

Slightly sweet

Applications

Solvent
Intermediate in pharmaceutical production
Chemical intermediate in synthesis of other compounds
Manufacturing of dyes
Manufacturing of pesticides
Component in hydraulic fluids and brake fluids

Hazards

Harmful if inhaled, swallowed, or comes into contact with skin
Flammable
Causes skin and eye irritation

Check Digit Verification of cas no

The CAS Registry Mumber 2203-35-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2203-35:
(6*2)+(5*2)+(4*0)+(3*3)+(2*3)+(1*5)=42
42 % 10 = 2
So 2203-35-2 is a valid CAS Registry Number.

2203-35-2Relevant academic research and scientific papers

A mild method for the replacement of a hydroxyl group by halogen. 1. Scope and chemoselectivity

Munyemana, Fran?ois,George, Isabelle,Devos, Alain,Colens, Alain,Badarau, Eduard,Frisque-Hesbain, Anne-Marie,Loudet, Aurore,Differding, Edmond,Damien, Jean-Marie,Rémion, Jeanine,Van Uytbergen, Jacqueline,Ghosez, Léon

, p. 420 - 430 (2015/12/31)

α-Chloro-, bromo- and iodoenamines, which are readily prepared from the corresponding isobutyramides have been found to be excellent reagents for the transformation of a wide variety of alcohols or carboxylic acids into the corresponding halides. Yields are high and conditions are very mild thus allowing for the presence of sensitive functional groups. The reagents can be easily tuned allowing therefore the selective monohalogenation of polyhydroxylated molecules. The scope and chemoselectivity of the reactions have been studied and reaction mechanisms have been proposed.

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