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(2S)-5,6-dioxo-2,4-dihydro-1H-indole-2-carboxylic acid is a chemical compound with a molecular formula C9H7NO4. It is a derivative of the indole-2-carboxylic acid and is characterized by its white to off-white crystalline powder form.

89762-39-0

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89762-39-0 Usage

Uses

Used in Pharmaceutical Industry:
(2S)-5,6-dioxo-2,4-dihydro-1H-indole-2-carboxylic acid is used as a key intermediate in the synthesis of various drugs, particularly for the development of anti-inflammatory and antiviral medications. Its unique structure and properties make it a valuable component in the creation of effective pharmaceuticals.
Used in Biochemistry and Medicinal Chemistry Research:
(2S)-5,6-dioxo-2,4-dihydro-1H-indole-2-carboxylic acid also has potential applications in the fields of biochemistry and medicinal chemistry. It serves as a significant compound for research and development purposes, contributing to the advancement of scientific knowledge and the discovery of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 89762-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,6 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89762-39:
(7*8)+(6*9)+(5*7)+(4*6)+(3*2)+(2*3)+(1*9)=190
190 % 10 = 0
So 89762-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO4/c11-7-2-4-1-6(9(13)14)10-5(4)3-8(7)12/h1,3,6,10H,2H2,(H,13,14)/t6-/m0/s1

89762-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dopachrome

1.2 Other means of identification

Product number -
Other names 5,6-dioxo-2,3,5,6-tetrahydro-indole-2-carboxylic acid

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:89762-39-0 SDS

89762-39-0Relevant academic research and scientific papers

An efficient preparation of mulberroside a from the branch bark of mulberry and its effect on the inhibition of tyrosinase activity

Wang, Shu,Liu, Xian-Ming,Zhang, Jian,Zhang, Yu-Qing

, (2015/02/19)

A bioactive ingredient in an ethanol extract from the branch bark of cultivated mulberry Husang-32 (Morus multicaulis Perr.) was isolated using a macroporous resin column. The primary component, which was purified by semi-preparative highperformance liqui

Continuous-flow step gradient mass spectrometry based method for the determination of kinetic parameters of immobilized mushroom tyrosinase in equilibrating conditions: Comparison with free enzyme

Salwinski, Aleksander,Delepee, Raphael,Maunit, Benot

experimental part, p. 3549 - 3554 (2012/03/27)

A mass spectrometry (MS)-based methodology for enzymatic assay in equilibrium conditions was designed and evaluated. This on-line assay involves the introduction of a continuous-flow step gradient (CFSG) of a substrate solution in the column containing immobilized enzyme and the simultaneous tracking of the product formation. We showed that the constant concentration of substrate in the entire bioreactor for an appropriate duration ensures the equilibration of the studied enzyme (mushroom tyrosinase). Under these conditions, it was demonstrated also that the kinetic and enzymatic parameters (Michaelis-Menten constant, KM, the maximal specific activity, SAmax) are independent of the flow rate of the mobile phase. The feasibility of the mentioned approach for inhibitory tests was also investigated. The coupling of the mass spectrometer to the bio-reactor allows the selective monitoring of the enzymatic reaction products and increases their detection level. Very high sensitivity, 500 pmol/min/column, and selective monitoring of the products of the enzymatic reaction are allowed by MS detection. The methodology developed here constitutes a sensitive analytical tool to study enzymes requiring long equilibration times. Copyright

HAIR DYE COMPOSITION

-

Page/Page column 11; 16, (2008/06/13)

An air-oxidative type hair dye composition containing a melanin precursor prepared by a process including (A) an oxidation step for converting, into the melanin precursor, a tyrosine or derivative thereof used as a starting substance with an enzyme or cell that is derived from a fungus selected from the group consisting of fungi belonging to the genera Aspergillus, Neurospora, Rhizomucor, Trichoderma, and Penicillium and that exhibits a catechol oxidase activity.

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