883907-83-3 Usage
Uses
Used in Pharmaceutical Industry:
2,2-dimethyl-oxazolidine-3,4-dicarboxylic acid 3-tert-butyl ester 4-ethyl ester is used as a precursor in organic synthesis for the development of pharmaceutical compounds. Its unique structure and functional groups may contribute to the creation of new drugs with specific therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 2,2-dimethyl-oxazolidine-3,4-dicarboxylic acid 3-tert-butyl ester 4-ethyl ester serves as a building block for constructing more complex molecules. Its ester groups and oxazolidine ring can be utilized in various chemical reactions to form a wide range of organic compounds.
Safety Considerations:
Due to the complex structure and potential reactivity of 2,2-dimethyl-oxazolidine-3,4-dicarboxylic acid 3-tert-butyl ester 4-ethyl ester, it is crucial to handle 2,2-dimethyl-oxazolidine-3,4-dicarboxylic acid 3-tert-butyl ester 4-ethyl ester with care and adhere to proper safety protocols during its synthesis, storage, and use.
Check Digit Verification of cas no
The CAS Registry Mumber 883907-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,9,0 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 883907-83:
(8*8)+(7*8)+(6*3)+(5*9)+(4*0)+(3*7)+(2*8)+(1*3)=223
223 % 10 = 3
So 883907-83-3 is a valid CAS Registry Number.
883907-83-3Relevant articles and documents
The Baylis-Hillman reaction with chiral α-amino aldehydes under racemization-free conditions
Coelho, Fernando,Diaz, Gaspar,Abella, Carlos A. M.,Almeida, Wanda P.
, p. 435 - 439 (2007/10/03)
The Baylis-Hillman reaction with chiral α-amino aldehydes has been revisited. The reaction carried out under the influence of ultrasound avoids the aldehyde racemization almost completely, providing useful chiral substrates which can be used as starting materials for the synthesis of natural products. To demonstrate the synthetic applicability of these adducts, the easy preparation of a bicyclic lactam with an indolizidinic skeleton was accomplished. Georg Thieme Verlag Stuttgart.
