40058-87-5 Usage
Description
Isopropyl 2-chloropropionate is a colorless liquid with a pungent odor. It has a density approximately equal to that of water and is insoluble in water. The flash point of this compound is near 50°F, and its vapors are heavier than air. It may be toxic if ingested or absorbed through the skin.
Uses
Used in Chemical Synthesis:
Isopropyl 2-chloropropionate is used as an intermediate in the chemical synthesis of various organic compounds. Its unique chemical structure allows it to be a versatile building block for creating a wide range of products.
Used in Pharmaceutical Industry:
Isopropyl 2-chloropropionate is used as a synthetic building block for the development of new pharmaceuticals. Its reactivity and functional groups make it a valuable component in the synthesis of various drug molecules.
Used in Agrochemical Industry:
Isopropyl 2-chloropropionate is used as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its properties enable it to be a key component in the formulation of these products.
Used in Flavor and Fragrance Industry:
Isopropyl 2-chloropropionate is used as a component in the creation of various flavors and fragrances. Its unique odor and reactivity make it a valuable addition to the development of new scents and tastes.
Used in Industrial Solvents:
Due to its solubility properties and low toxicity, isopropyl 2-chloropropionate can be used as a solvent in various industrial applications, such as cleaning agents, degreasers, and paint removers.
Air & Water Reactions
Highly flammable. Insoluble in water.
Reactivity Profile
ISOPROPYL CHLOROPROPIONATE is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.
Health Hazard
May cause toxic effects if inhaled or absorbed through skin. Inhalation or contact with material may irritate or burn skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.
Fire Hazard
HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
Check Digit Verification of cas no
The CAS Registry Mumber 40058-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,0,5 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40058-87:
(7*4)+(6*0)+(5*0)+(4*5)+(3*8)+(2*8)+(1*7)=95
95 % 10 = 5
So 40058-87-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H11ClO2/c1-4(2)9-6(8)5(3)7/h4-5H,1-3H3
40058-87-5Relevant articles and documents
Synthesis of diaryl acetates and oxindoles via a sequential VNS Ar-SNAr three-component coupling reaction
Lawrence, Nicholas J.,Davies, Christopher A.,Gray, Matthew
, p. 4957 - 4960 (2004)
(Chemical Equation Presented) The VNS and SNAr reactions combine to form an efficient three-component one-pot route to diarylmethanes. The products of selected diaryl acetates provide modular 3-aryloxindole derivatives.
Process for the preparation of an alkyl 2-chloropropionate by chlorinating an alkyl lactate
-
, (2008/06/13)
A racemic or optically active alkyl 2-chloropropionate is prepared, respectively, from a racemic or optically active alkyl lactate by, in a first step, gradually bringing the alkyl lactate into contact with the thionyl chloride, in the presence of an organic base, while maintaining, in the reaction mixture, an excess of thionyl chloride, relative to the amount of alkyl lactate introduced into this mixture, at a temperature below the decomposition point of the chlorosulphinate of the alkyl lactate, which is formed as an intermediate, and then, in a second step, in heating the reaction mixture resulting from the first step at a temperature which is at least equal to the decomposition point of the chlorosulphinate of the alkyl lactate. The alkyl 2-chloropropionates can be used for the manufacture of the racemic or optically active 2-phenoxypropionic acids.
