13208-96-3 Usage
Description
(3Z)-7-METHYL-1H-INDOLE-2,3-DIONE 3-OXIME is a chemical compound that belongs to the class of oxime derivatives. It is a yellow solid with a molecular formula C10H8N2O2 and a molecular weight of 184.18 g/mol. (3Z)-7-METHYL-1H-INDOLE-2,3-DIONE 3-OXIME has potential applications in the fields of pharmaceuticals and organic synthesis due to its oxime group and indole-dione core structure, which provide it with the potential to act as a chelating agent and exhibit various pharmacological properties.
Uses
Used in Pharmaceutical Industry:
(3Z)-7-METHYL-1H-INDOLE-2,3-DIONE 3-OXIME is used as a starting material for the development of new compounds with biological activity. Its oxime group allows it to act as a chelating agent, enabling it to form complexes with metal ions, which can be useful in the development of drugs with specific therapeutic effects.
Used in Organic Synthesis:
(3Z)-7-METHYL-1H-INDOLE-2,3-DIONE 3-OXIME is used as an intermediate in the synthesis of various organic compounds. Its indole-dione core structure provides a versatile platform for chemical modifications, allowing for the development of new compounds with potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 13208-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,0 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13208-96:
(7*1)+(6*3)+(5*2)+(4*0)+(3*8)+(2*9)+(1*6)=83
83 % 10 = 3
So 13208-96-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O2/c1-5-3-2-4-6-7(5)10-9(12)8(6)11-13/h2-4,13H,1H3,(H,10,11,12)
13208-96-3Relevant articles and documents
Synthesis of isatin 3-oximes from 2-nitroacetanilides
Kearney,Harris,Jackson,Joule
, p. 769 - 772 (2007/10/02)
2-Nitroacetanilides, prepared by alkaline hydrolysis of 1-arylamino-1-methylthio-2-nitroethenes, are converted into isatin (1H-indole-2,3-dione) 3-oximes by treatment with concentrated sulfuric acid or trifluoromethanesulfonic acid at room temperature.
