62965-56-4 Usage
Description
(S)-(-)-4-tert-Butyloxazolidine-2,5-dione is an organic compound that serves as a crucial intermediate in various chemical and pharmaceutical processes. It is characterized by its unique molecular structure, which includes a tert-butyl group and an oxazolidine ring fused to a dione moiety. This structure endows it with specific reactivity and properties that make it valuable in the synthesis of complex molecules and pharmaceutical agents.
Uses
Used in Organic Synthesis:
(S)-(-)-4-tert-Butyloxazolidine-2,5-dione is used as a key intermediate for the synthesis of various organic compounds. Its unique structure allows for selective functionalization and modification, making it a versatile building block in the construction of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (S)-(-)-4-tert-Butyloxazolidine-2,5-dione is utilized as a starting material or intermediate in the development of new drugs. Its reactivity and structural features enable the creation of novel bioactive molecules with potential therapeutic applications.
Used in Agrochemicals:
(S)-(-)-4-tert-Butyloxazolidine-2,5-dione is also employed in the agrochemical sector as a precursor for the synthesis of various agrochemical products, such as pesticides and herbicides. Its unique properties allow for the development of new compounds with improved efficacy and selectivity.
Used in Dye Industry:
In the dye industry, (S)-(-)-4-tert-Butyloxazolidine-2,5-dione is used as a raw material for the production of various dyes and pigments. Its structural features contribute to the development of dyes with enhanced color properties and stability.
Check Digit Verification of cas no
The CAS Registry Mumber 62965-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,6 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62965-56:
(7*6)+(6*2)+(5*9)+(4*6)+(3*5)+(2*5)+(1*6)=154
154 % 10 = 4
So 62965-56-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO3/c1-7(2,3)4-5(9)11-6(10)8-4/h4H,1-3H3,(H,8,10)
62965-56-4Relevant articles and documents
ENANTIOSELECTIVE SYNTHESIS OF NON-PROTEINOGENIC AMINO ACIDS VIA METALLATED BIS-LACTIM ETHERS OF 2,5-DIKETOPIPERAZINES
Schoellkopf, Ulrich
, p. 2085 - 2092 (2007/10/02)
Bis-lactim ethers 1 of 2,5-diketopiperazines contain a chiral inducing center, an acidic CH-bond and two sites susceptible to hydrolysis.They react with BuLi to give Li compounds of type 4, 15, 29 or 32, which possess a prochiral C atom.They readily add electrophiles (such as alkylating agents or carbonyl compounds) with unusually high diastereoface differentiation.In many cases the d.e-value (d.e. = diastereomeric excess = asymmetric induction) of the adduct exceeds 95percent.On hydrolysis the adducts are cleaved liberating the chiral auxiliary (used to build up the bis-lactim ether 1) and the target molecules, the optically active amino acid methyl esters of type 8, 19, 25 or 36.The two amino acid esters are separable either by fractional distillation or (eventually after further hydrolysis to amino acids) by chromatography.Transition state models are discussed that could explain the exceptionally high asymmetric induction and the predictability of the induced configuration.
