770746-47-9 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Diazabicyclo[4.2.0]octane-3,5-dione is utilized as a catalyst in the pharmaceutical industry for its ability to facilitate acylation reactions, which are essential in the synthesis of various drug compounds. Its high reactivity and selectivity ensure the efficient production of desired pharmaceuticals with minimal side reactions.
Used in Polymer Industry:
In the polymer industry, 2,4-Diazabicyclo[4.2.0]octane-3,5-dione serves as a catalyst to enhance the formation of polymers through acylation reactions. This role is critical in the development of specific polymer properties, contributing to the advancement of material science.
Used in Pesticide Production:
2,4-Diazabicyclo[4.2.0]octane-3,5-dione is employed as a catalyst in the production of pesticides, where its ability to promote acylation reactions aids in the synthesis of active ingredients that are effective in controlling pests and ensuring crop protection.
Used in Dye Production:
Within the dye industry, 2,4-Diazabicyclo[4.2.0]octane-3,5-dione is used as a catalyst to expedite acylation reactions necessary for the synthesis of various dyes. Its catalytic properties are harnessed to produce dyes with specific characteristics, catering to the diverse needs of different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 770746-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,0,7,4 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 770746-47:
(8*7)+(7*7)+(6*0)+(5*7)+(4*4)+(3*6)+(2*4)+(1*7)=189
189 % 10 = 9
So 770746-47-9 is a valid CAS Registry Number.
770746-47-9Relevant academic research and scientific papers
[2+2] Photocycloadditions with chiral uracil derivatives: Access to all four stereoisomers of 2-aminocyclobutanecarboxylic acid
Fernandes, Carlos,Gauzy, Christine,Yang, Yi,Roy, Olivier,Pereira, Elisabeth,Faure, Sophie,Aitken, David J.
, p. 2222 - 2232 (2008/03/28)
Starting from a single, chiral, bicyclic derivative of uracil, all four stereoisomers of 2-aminocyclobutanecarboxylic acid have been prepared in enantiomerically pure form, using a synthetic sequence which begins with a key photochemical [2+2] cycloaddition reaction and includes a practical cis to trans β-amino acid isomerisation procedure. Georg Thieme Verlag Stuttgart.
Synthesis of (+)-(1S,2R) and (-)-(1R,2S)-2-aminocyclobutane-1-carboxylic acids
Gauzy, Christine,Pereira, Elisabeth,Faure, Sophie,Aitken, David J.
, p. 7095 - 7097 (2007/10/03)
(+)-(1S,2R) and (-)-(1R,2S)-2-aminocyclobutane-1-carboxylic acids have been prepared in >97% ee and in 33% and 20% overall yields starting from a single, chiral, bicyclic compound perceived as a chiral uracil equivalent. Construction of the cyclobutane ri
