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(3Z)-5-METHYL-1H-INDOLE-2,3-DIONE 3-OXIME is an indole-based chemical compound that belongs to the class of oxime derivatives. It has a molecular formula of C10H9NO2 and consists of a 5-methyl-1H-indole-2,3-dione core with an oxime functional group attached at the 3-position. (3Z)-5-METHYL-1H-INDOLE-2,3-DIONE 3-OXIME has potential applications in various fields including pharmaceuticals, biochemistry, and organic synthesis, and may exhibit interesting biological activities.

13208-98-5

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13208-98-5 Usage

Uses

Used in Pharmaceutical Industry:
(3Z)-5-METHYL-1H-INDOLE-2,3-DIONE 3-OXIME is used as a drug candidate for its potential biological activities and further development in the field of pharmaceuticals.
Used in Biochemistry:
(3Z)-5-METHYL-1H-INDOLE-2,3-DIONE 3-OXIME is used as a building block for the synthesis of other biologically active compounds in biochemistry research.
Used in Organic Synthesis:
(3Z)-5-METHYL-1H-INDOLE-2,3-DIONE 3-OXIME is used as a key intermediate in the synthesis of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 13208-98-5 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 13208-98:
(7*1)+(6*3)+(5*2)+(4*0)+(3*8)+(2*9)+(1*8)=85
85 % 10 = 5
So 13208-98-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O2/c1-5-2-3-7-6(4-5)8(11-13)9(12)10-7/h2-4,13H,1H3,(H,10,11,12)

13208-98-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(hydroxyamino)-5-methylindol-2-one

1.2 Other means of identification

Product number -
Other names 5-methyl-indoline-2,3-dione-3-oxime

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13208-98-5 SDS

13208-98-5Relevant academic research and scientific papers

Acylating and arylsulfonylating ability of O-derivatives of isatin 3-oximes

Stankevicius,Terentiev,Janushene,Savickas

, p. 98 - 104 (2007/10/03)

O-Acyl and O-arylsulfonyl derivatives of isatin 3-oximes have been synthesized and their interaction with alcohols and amines has been investigated. It was established that none of the esters of 1-substituted isatin 3-oximes reacted with the indicated nucleophiles. 1-Unsubstituted O-aryl and O-arylsulfonyl derivatives react with amines as acylating agents even at room temperature, but O-acetyl derivatives only on heating. Acylamides or arylsulfamides respectively are formed in this way. O-Acyl derivatives do not react with alcohols at room temperature. Only O-benzoyl derivatives form ethyl benzoate on heating in ethanol. A comparative analysis of mass spectrometric data on the processes of acylation and arylsulfonylation is given.

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.

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