104605-97-2 Usage
Description
(R)-2-((4-FLUOROPHENOXY)METHYL)OXIRANE is an epoxide compound with a molecular formula of C9H9FO2. It is a chiral compound, meaning it has two stereoisomers, with the (R)-enantiomer being the one specified in the name. (R)-2-((4-FLUOROPHENOXY)METHYL)OXIRANE contains a fluorophenyl group and an oxirane group, which is a three-membered ring containing one oxygen atom. Its structure and properties make it valuable in the development of new drugs and biologically active molecules.
Uses
Used in Pharmaceutical Industry:
(R)-2-((4-FLUOROPHENOXY)METHYL)OXIRANE is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the creation of new drugs and biologically active molecules, contributing to the development of novel treatments for various medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, (R)-2-((4-FLUOROPHENOXY)METHYL)OXIRANE is used as a key component in the synthesis of agrochemicals. Its properties make it suitable for the development of new pesticides, herbicides, and other agricultural chemicals that can help improve crop yields and protect plants from pests and diseases.
Used in Material Science:
(R)-2-((4-FLUOROPHENOXY)METHYL)OXIRANE is also utilized in the field of material science. Its high reactivity and specificity make it an ideal reagent for chemical reactions, leading to the development of new materials with specific properties for various applications, such as in electronics, coatings, and adhesives.
Used as a Reagent in Chemical Reactions:
Due to its high reactivity and specificity, (R)-2-((4-FLUOROPHENOXY)METHYL)OXIRANE is often used as a reagent in chemical reactions. This allows for the synthesis of a wide range of compounds with specific properties, which can be applied in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 104605-97-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,0 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104605-97:
(8*1)+(7*0)+(6*4)+(5*6)+(4*0)+(3*5)+(2*9)+(1*7)=102
102 % 10 = 2
So 104605-97-2 is a valid CAS Registry Number.
104605-97-2Relevant articles and documents
A new synthesis of sultams from amino alcohols
Lad, Nitin,Sharma, Rajiv,Marquez, Victor E.,Mascarenhas, Malcolm
, p. 6307 - 6309 (2013)
The base-mediated cyclization of N,O-dimesylate derivatives of cyclic and acyclic amino alcohols provides a simple access to five- and six-member sultams: isothiazolidine-1,1-dioxides and thiazinane-1,1-dioxides respectively.
Montmorillonite K10 catalyzed highly regioselective azidolysis of epoxides: A short and efficient synthesis of phenylglycine
Ch Ghosh, Keshab,Banerjee, Isita,Sinha, Surajit
supporting information, p. 2923 - 2934 (2018/12/04)
A series of β‐hydroxyazides were effectively synthesized from the regioselective ring opening of epoxides by sodium azide using montmorillonite K10 as a novel heterogeneous catalyst in aqueous acetonitrile in good to excellent yields. The utility of this method has been demonstrated by achieving a short synthesis of phenylglycine in 33.5% overall yield.
Solvent-Directed Epoxide Opening with Primary Amines for the Synthesis of β-Amino Alcohols
Lizza, Joseph R.,Moura-Letts, Gustavo
supporting information, p. 1231 - 1242 (2017/03/11)
An efficient synthesis of β-amino alcohols from a variety of epoxides and primary unbranched amines in the absence of any catalyst in high yields and regioselectivities is reported. A variety of polar mixed solvent systems allow for the selective formation of secondary amino alcohols over tertiary amino alcohols. The reaction scope extends to a wide variety of aromatic and aliphatic substituted epoxides and primary amines bearing complex functionality.
