131362-99-7 Usage
Family
Isoxazolecarboxaldehyde
Configuration
cis
Structure
Consists of a 3-isoxazole ring fused with a carboxaldehyde group and a 4,5-dihydro-4-methyl-5-(1-methylethyl) side chain
Applications
May have applications in various chemical and pharmaceutical processes
Handling
It is important to handle and use this chemical with care, following safety guidelines and regulations to prevent any potential hazards or risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 131362-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,6 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 131362-99:
(8*1)+(7*3)+(6*1)+(5*3)+(4*6)+(3*2)+(2*9)+(1*9)=107
107 % 10 = 7
So 131362-99-7 is a valid CAS Registry Number.
131362-99-7Relevant academic research and scientific papers
Lewis Acid Promoted Stereoselective Carbon-Carbon Bond Formation of 3-Formyl-Δ2-isoxazolines
Kamimura, Akio,Yoshihara, Kosei,Marumo, Shinji,Yamamoto, Akinori,Nishiguchi, Takeshi,et al.
, p. 5403 - 5413 (2007/10/02)
4,5-Disubstituted 3-formyl-Δ2-isoxazolines undergo the aldol, allylation, and carbonyl ene reactions in the presence of appropriate Lewis acid to give the adducts with an effective 1,3-asymmetric induction.The stereoselectivity of the reaction
