165657-74-9

Basic information

• Product Name: (R)-4-(2-IODO-ETHYL)-2,2-DIMETHYL-[1,3]DIOXOLANE
• Synonyms: (R)-4-(2-IODO-ETHYL)-2,2-DIMETHYL-[1,3]DIOXOLANE
• CAS NO: 165657-74-9
• Molecular Formula: C₇H₁₃IO₂
• Molecular Weight: 256.08
• Mol File: 165657-74-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R)-4-(2-IODO-ETHYL)-2,2-DIMETHYL-[1,3]DIOXOLANE(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-4-(2-IODO-ETHYL)-2,2-DIMETHYL-[1,3]DIOXOLANE(165657-74-9)
• EPA Substance Registry System: (R)-4-(2-IODO-ETHYL)-2,2-DIMETHYL-[1,3]DIOXOLANE(165657-74-9)

Safety Data

• Hazardous Substances Data: 165657-74-9(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(R)-4-(2-IODO-ETHYL)-2,2-DIMETHYL-[1,3]DIOXOLANE is used as a reagent in organic synthesis for its ability to facilitate the formation of complex organic compounds. Its unique structure with a chiral center and functional groups makes it a valuable component in creating a wide range of molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (R)-4-(2-IODO-ETHYL)-2,2-DIMETHYL-[1,3]DIOXOLANE is used as an intermediate in the production of various drugs. Its structural properties allow it to be a key building block in the synthesis of medicinal compounds, contributing to the development of new and improved pharmaceuticals.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, (R)-4-(2-IODO-ETHYL)-2,2-DIMETHYL-[1,3]DIOXOLANE serves as an intermediate for the synthesis of different agrochemicals. Its role in creating complex molecules aids in the development of more effective and targeted products for agricultural applications.
Used in Research and Development:
(R)-4-(2-IODO-ETHYL)-2,2-DIMETHYL-[1,3]DIOXOLANE is also utilized in research and development settings as a building block for the synthesis of more complex organic compounds. Its unique structure and properties make it an attractive candidate for exploring new chemical reactions and creating novel molecules with potential applications in various fields.

Upstream product

• 165657-75-0 (4R)-2-(2,2-Dimethyl-1,3-dioxolan-4-yl)ethyl 4-methylbenzenesulfonate 
• 5754-34-7 2-((4R)-2,2-dimethyl-1,3-dioxolan-4-yl)ethanol 

Downstream Products

• 165876-49-3 (2R,5R,2'S,5'S)-5-<5'-<(tert-butyldiphenylsiloxy)methyl>tetrahydro-2'-furyl>-1,2-O-isopropylidenepentane-1,2,5-triol 
• 149099-16-1 (2R,5S,2'S,5'S)-5-<5'-<(tert-Butyldiphenylsiloxy)methyl>tetrahydrofuran-2'-yl>-1,2-O-isopropylidenepentane-1,2,5-triol 
• 1312441-90-9 C₂₉H₄₆O₆ 
• 1312441-91-0 C₂₉H₄₈O₆ 
• 1312441-92-1 C₃₇H₅₄O₇ 
• 1312442-02-6 C₃₇H₅₆O₇ 
• 1312441-93-2 C₃₇H₅₆O₇ 
• 1312442-04-8 C₄₇H₆₃F₃O₉ 
• 1312442-03-7 C₄₇H₆₃F₃O₉ 
• 1312441-94-3 C₃₉H₆₀O₈ 
• 1312441-89-6 C₂₀H₃₁NO₄ 

Relevant articles and documents

METHODS FOR SYNTHESIS OF RESOLVINS

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AMINO GROUP-CONTAINING PYRROLIDINONE DERIVATIVE

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The first total synthesis of cytopiloyne, an anti-diabetic, polyacetylenic glucoside

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Stereoselective Additions of Chiral, Functionalized Organozinc Reagents to Achiral and Chiral Aldehydes: a Matched-Mismatched Case in Organozinc Chemistry

The additions of the enantiomerically pure organozinc reagents 17 and 33 to the THF-aldehyde 1 in the presence of the monodentate Lewis acid boron trifluoride-ether give the nonchelation-controlled addition products 7 and 36, respectively (stereoselectivity 95:5, 86:14).These results provide a route to oligo(tetrahydrofuran)s with the relative stereochemistry trans-syn-cis.A stereodirecting effect of the chiral center in the organozinc reagent 17 is found, leading to simple diastereoselectivies in the reaction with achiral aldehydes and to a matched-mismatched case in the reaction with the chiral aldehyde 1. - Key Words: Addition, stereoselective, nonchelation-controlled / Reagent, organozinc / Stereodifferentiation, double / Oligo(tetrahydrofuran)