210641-50-2 Usage
General Description
3-Isoxazolecarboxamide, 4,5-dihydro-5-(hydroxymethyl)-N-methyl-(9CI) is a chemical compound with the molecular formula C7H10N2O3. It is also known by its IUPAC name, 4,5-dihydro-5-(hydroxymethyl)-N-methyl-3-isoxazolecarboxamide. 3-Isoxazolecarboxamide,4,5-dihydro-5-(hydroxymethyl)-N-methyl-(9CI) is a derivative of isoxazole and carboxamide, and it has potential applications in the pharmaceutical industry. Its structure contains a five-membered ring with oxygen and nitrogen atoms, as well as a methyl group and a hydroxymethyl group attached to the ring. The combination of these functional groups makes 3-Isoxazolecarboxamide,4,5-dihydro-5-(hydroxymethyl)-N-methyl-(9CI) interesting for further study and potential development for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 210641-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,6,4 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 210641-50:
(8*2)+(7*1)+(6*0)+(5*6)+(4*4)+(3*1)+(2*5)+(1*0)=82
82 % 10 = 2
So 210641-50-2 is a valid CAS Registry Number.
210641-50-2Relevant academic research and scientific papers
An anomalous hydration/dehydration sequence for the mild generation of a nitrile oxide
Nishiwaki, Nagatoshi,Kobiro, Kazuya,Kiyoto, Hideyuki,Hirao, Shotaro,Sawayama, Jun,Saigo, Kazuhiko,Okajima, Yoshikazu,Uehara, Toshiharu,Maki, Asaka,Ariga, Masahiro
experimental part, p. 2832 - 2839 (2011/05/04)
A nitrile oxide containing a carbamoyl group is readily generated upon the treatment of 2-methyl-4-nitro-3-isoxazolin-5(2H)-one with water under mild reaction conditions, even in the absence of special reagents. The obtained nitrile oxide undergoes cycloa
Improved generation method for functionalized nitrile oxide
Nishiwaki, Nagatoshi,Uehara, Toshiharu,Asaka, Noriko,Tohda, Yasuo,Ariga, Masahiro,Kanemasa, Shuji
, p. 4851 - 4852 (2007/10/03)
Gentle generation of nitrile oxide bearing a carbamoyl group was performed. 4-Nitro-3-isoxazolin-5-one was treated with dipolarophiles in the mixed solvent (MeCN/H2O) at room temperature to afford cycloadducts in good yields.
