10365-13-6 Usage
General Description
1,2-bis(2,5-dimethoxyphenyl)ethane-1,2-dione, also known as DME-1,2-dione, is a chemical compound used in organic synthesis and as a reagent in chemical reactions. It is a diketone compound with two aromatic rings, making it highly reactive and useful in the production of various organic compounds. DME-1,2-dione is also a useful building block in the preparation of pharmaceuticals and agrochemicals. It is known for its ability to form complex molecular structures, making it an important intermediate in the synthesis of more complex organic molecules. Its unique molecular structure allows for the formation of diverse chemical compounds, making it a valuable and versatile chemical in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 10365-13-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,6 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10365-13:
(7*1)+(6*0)+(5*3)+(4*6)+(3*5)+(2*1)+(1*3)=66
66 % 10 = 6
So 10365-13-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H18O6/c1-21-11-5-7-15(23-3)13(9-11)17(19)18(20)14-10-12(22-2)6-8-16(14)24-4/h5-10H,1-4H3
10365-13-6Relevant articles and documents
Ring Closing Metathesis Approach for the Synthesis of o-Terphenyl Derivatives
Karmakar, Shilpi,Mandal, Tirtha,Dash, Jyotirmayee
, p. 5916 - 5924 (2019/08/21)
A linear synthesis of o-terphenyl derivatives has been delineated using ring closing metathesis (RCM) as the key step. In this approach, benzil derivatives upon allyl Grignard addition provides diphenyl-1,2-diallyl dihydroxy derivatives which undergo ring closing metathesis to afford tetrahydro terphenyl derivatives. Aromatization-driven dehydration then leads to a diverse set of electron rich and electron deficient o-terphenyls. Furthermore, oxidative coupling of electron rich o-terphenyls provides the corresponding triphenylene derivatives.
