33717-87-2 Usage
Description
1-Oxaspiro[2.5]octane-2-carboxylic acid, methyl ester (7CI, 8CI, 9CI) is a chemical compound with the molecular formula C8H14O3. It is a methyl ester derivative of a spiro compound, featuring a bicyclic ring system with an oxygen atom bridging the two rings. This unique chemical structure endows it with potential pharmacological properties, making it a promising candidate for various applications in different fields.
Uses
Used in Pharmaceutical Synthesis:
1-Oxaspiro[2.5]octane-2-carboxylic acid, methyl ester (7CI, 8CI, 9CI) is used as an intermediate in the synthesis of pharmaceuticals for its unique chemical structure and potential biological activity. It plays a crucial role in the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Synthesis:
In the agrochemical industry, 1-Oxaspiro[2.5]octane-2-carboxylic acid, methyl ester (7CI, 8CI, 9CI) is utilized as a key component in the synthesis of various agrochemicals. Its incorporation aids in the development of innovative products with enhanced performance and reduced environmental impact.
Used in Organic Compound Synthesis:
1-Oxaspiro[2.5]octane-2-carboxylic acid, methyl ester (7CI, 8CI, 9CI) is also employed in the synthesis of other organic compounds, showcasing its versatility and potential applications across a wide range of chemical processes. Its unique structure allows for the creation of novel compounds with diverse properties and uses.
Used in Drug Development Research:
Due to its promising biological activity demonstrated in certain research studies, 1-Oxaspiro[2.5]octane-2-carboxylic acid, methyl ester (7CI, 8CI, 9CI) is used as a subject of investigation in drug development research. Scientists explore its potential applications in treating various diseases and conditions, aiming to harness its unique properties for therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 33717-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,1 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33717-87:
(7*3)+(6*3)+(5*7)+(4*1)+(3*7)+(2*8)+(1*7)=122
122 % 10 = 2
So 33717-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O3/c1-11-8(10)7-9(12-7)5-3-2-4-6-9/h7H,2-6H2,1H3
33717-87-2Relevant articles and documents
Carboxylate-stabilised sulfur ylides (thetin salts) in asymmetric epoxidation for the synthesis of glycidic acids. Mechanism and implications
Aggarwal, Varinder K.,Hebach, Christina
, p. 1419 - 1427 (2007/10/03)
The reaction of carboxylate-stabilised sulfur ylides (thetin salts) with aldehydes and ketones has been investigated. Using both achiral and chiral sulfur ylides, good yields were obtained with dimsylsodium or LHMDS as bases in DMSO or THF-DMSO mixtures.
A convenient synthesis of aziridine-2-carboxylic esters
Legters, Johan,Thijs, Lambertus,Zwanenburg, Binne
, p. 1 - 15 (2007/10/02)
Optically active oxirane-2-carboxylic esters, prepared from allylic alcohols employing the Sharpless epoxidation, were treated with sodium azide.The azido alcohols obtained were subsequently converted into aziridine-2-carboxylic esters by reaction with triphenylphosphine, in good yields and with high optical purity.Various racemic oxirane-2-carboxylic esters were subjected to the same sequence of reactions.
ELECTROREDUCTIVE COUPLING OF METALLYLCHLORIDE OR METHYL CHLOROACETATE WITH CARBONYL COMPOUNDS CAATLYZED BY NICKEL BIPYRIDINE COMPLEXES
Sibille, Soline,d'Incan, Esther,Leport, Luis,Massebiau, Marie-Claude,Perichon, Jacques
, p. 55 - 58 (2007/10/02)
An efficient electrosynthesis of homoallyl alcohols or β-hydroxy esters in the presence of catalytic amounts of the NiBr2(2,2'-bipyridine) complex has been developed from mixed electrolysis of metellylchloride, or methyl chloroacetate with several carbonyl compounds, using a one-compartment cell equiped with a sacrificial zinc anode.
