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112632-98-1

1-acetyl-3-oxo-2,3-dihydro-1H-indol-2-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 112632-98-1 Structure

  • Basic information

    1. Product Name: 1-acetyl-3-oxo-2,3-dihydro-1H-indol-2-yl acetate
    2. Synonyms: 1-acetyl-3-oxo-2,3-dihydro-1H-indol-2-yl acetate
    3. CAS NO:112632-98-1
    4. Molecular Formula: C12H11NO4
    5. Molecular Weight: 233.22004
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112632-98-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-acetyl-3-oxo-2,3-dihydro-1H-indol-2-yl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-acetyl-3-oxo-2,3-dihydro-1H-indol-2-yl acetate(112632-98-1)
    11. EPA Substance Registry System: 1-acetyl-3-oxo-2,3-dihydro-1H-indol-2-yl acetate(112632-98-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 112632-98-1(Hazardous Substances Data)

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.

112632-98-1Downstream Products

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.

Direct C(sp3)-H acyloxylation of indolin-3-ones with carboxylic acids catalysed by KI

Cao, Zhuo-Xian,Duan, Dong-Zhu,Fei, Xing-Hai,He, Bin,Tang, Yong-Qin,Yang, Fen-Fen,Yang, Yuan-Yong,Zhao, Qing-Jie,Zhao, Yong-Long,Zhou, Meng

supporting information, p. 2354 - 2358 (2020/05/19)

The first KI-catalyzed direct acyloxylation of indolin-3-ones with carboxylic acids has been developed using 30% aq. H2O2 as a green oxidant at room temperature. Through this strategy, various C2-acyloxy indolin-3-ones were obtained in up to 96% yield. Moreover, the C2-acyloxy indolin-3-ones can serve as versatile intermediates for the synthesis of nucleophilic 2-monoarylated indolin-3-ones and 3-ylidene indoles.

Construction method of N-acetyl-3-oxindole compound and C-O bond at C2 position of N-acetyl-3-oxindole compound

-

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

Oxidation of indoles and 1,2-dihydro-3H-indol-3-ones

Desarbre,Savelon,Cornec,Merour

, p. 2983 - 2994 (2007/10/03)

2-Hydroxy-1,2-dihydro-3H-indol-3-ones 3 were obtained from 1,2-dihydro-3H-indol-3-ones 2 by using various conditions (m-CPBA or sodium azide) depending on substituents in 1-position. The reactivity of hydroxyketones 3 is examined and oxidation of 1-(phenylsulfonyl)indole by m-CPBA is described.

RING-CHAIN TAUTOMERISM AND SOME REACTIONS OF 2-HYDROXYINDOLINE DERIATIVES

Kawasaki, Tomomi,Ohtsuka, Hiroaki,Chien, Chun-Sheng,Omata, Mitsugu,Sakamoto, Masanori

, p. 1339 - 1346 (2007/10/02)

The spectral (proton and carbon-13 nuclear magnetic resonance) and chemical properties of the 1-acetyl-2-hydroxyindoleins 1-5, which can exist in the ring (A) and chain (B) tautomers, have been investigated.The methylation and acetylation of the 2-hydroxy

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