112632-98-1 Usage
Indole derivative
A heterocyclic aromatic ring The compound contains an indole structure, which is a five-membered carbon ring fused to a six-membered nitrogen-containing ring.
Acetyl and acetate groups
Potential applications in medicinal chemistry The presence of these functional groups suggests that the compound may have specific biological activities, making it suitable for pharmaceutical and organic compound synthesis.
Versatile compound
Potential pharmaceutical and industrial uses Due to its unique structure and functional groups, 1-acetyl-3-oxo-2,3-dihydro-1H-indol-2-yl acetate can be used in various applications, including the synthesis of pharmaceuticals and other organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 112632-98-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,3 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112632-98:
(8*1)+(7*1)+(6*2)+(5*6)+(4*3)+(3*2)+(2*9)+(1*8)=101
101 % 10 = 1
So 112632-98-1 is a valid CAS Registry Number.
112632-98-1Relevant articles and documents
REARRANGEMENT OF 1-ACETYLINDOXYL OXIME INTO 1-ACETYL-2-ACETOXY-3-IMINOINDOLINE HYDROSULFATE
Velezheva, V. S.,Rabova, S. Yu.,Alekseeva, L. M.
, p. 279 - 281 (1990)
1-Acetyl-2-acetoxy-3-iminoindoline hydrosulfate was obtained by rearrangement of 1-acetylindoxyl oxime by the action of concentrated H2SO4.The hydrolysis and oxidative dimerization reactions of the above iminoindoline hydrosulfate were investigated.
Construction method of N-acetyl-3-oxindole compound and C-O bond at C2 position of N-acetyl-3-oxindole compound
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Paragraph 0056-0059; 0064-0067, (2020/04/06)
The invention discloses a construction method of an N-acetyl-3-oxindole compound and a C-O bond at the C2 position of the N-acetyl-3-oxindole compound, and belongs to the technical field of organic synthesis. A C2-position acylation reaction of a compound
1-ACETYL-2-BROMO-3-INDOLINONE IN NUCLEOPHILIC SUBSTITUTION REACTIONS AND THE SYNTHESIS OF PYRROLOINDOLES
Velezheva, V. S.,Mel'man, A. I.,Smushkevich, Yu. I.,Pol'shakov, V. I.,Anisimova, O. S.
, p. 917 - 923 (2007/10/02)
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