948594-94-3 Usage
Description
(S)-4-Chloro-1,2-epoxybutane, with the molecular formula C4H7ClO, is a colorless liquid chemical compound that belongs to the class of epoxides. It features a three-membered cyclic ether ring with a chloro group attached to the carbon atom within the ring. (S)-4-Chloro-1,2-epoxybutane is known for its reactivity, particularly in nucleophilic substitution reactions, and is widely utilized in organic synthesis for creating a variety of chemical products, including pharmaceuticals, agrochemicals, and other organic compounds. Furthermore, (S)-4-chloro-1,2-epoxybutane serves as a fundamental building block in the production of polymers and other materials. However, due to its potential toxicity and irritating properties, it is crucial to handle this compound with care to avoid skin, eye, and respiratory system irritation.
Uses
Used in Organic Synthesis:
(S)-4-Chloro-1,2-epoxybutane is used as a reagent in the field of organic synthesis for its ability to participate in nucleophilic substitution reactions. This characteristic makes it a valuable component in the creation of pharmaceuticals, agrochemicals, and other organic compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (S)-4-chloro-1,2-epoxybutane is utilized as a key intermediate in the synthesis of various medicinal compounds. Its reactivity allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Development:
(S)-4-Chloro-1,2-epoxybutane is also employed in the agrochemical sector, where it is used to synthesize compounds with pesticidal, herbicidal, or fungicidal properties, contributing to the development of more effective crop protection agents.
Used in Polymer Production:
In the polymer industry, (S)-4-chloro-1,2-epoxybutane serves as a building block for the production of various types of polymers. Its incorporation into polymer structures can enhance their properties, such as strength, durability, or chemical resistance, depending on the specific application.
Check Digit Verification of cas no
The CAS Registry Mumber 948594-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,8,5,9 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 948594-94:
(8*9)+(7*4)+(6*8)+(5*5)+(4*9)+(3*4)+(2*9)+(1*4)=243
243 % 10 = 3
So 948594-94-3 is a valid CAS Registry Number.
948594-94-3Relevant articles and documents
Scalable Total Synthesis, IP3R Inhibitory Activity of Desmethylxestospongin B, and Effect on Mitochondrial Function and Cancer Cell Survival
Podunavac, Ma?a,Mailyan, Artur K.,Jackson, Jeffrey J.,Lovy, Alenka,Farias, Paula,Huerta, Hernan,Molgó, Jordi,Cardenas, Cesar,Zakarian, Armen
, p. 11278 - 11282 (2021)
The scalable synthesis of the oxaquinolizidine marine natural product desmethylxestospongin B is based on the early application of Ireland–Claisen rearrangement, macrolactamization, and a late-stage installation of the oxaquinolizidine units by lactam reduction. The synthesis serves as the source of material to investigate calcium signaling and its effect on mitochondrial metabolism in various cell types, including cancer cells.
