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1H-Indole-5,6-dione, 2,3-dihydro-3-hydroxy-1-(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

3736-31-0

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3736-31-0 Usage

Physical appearance

Yellowish crystalline compound

Derivative of

Indole

Uses

Synthesis of various pharmaceuticals

Known for

Antiviral, antibacterial, and anticancer properties

Potential as

Neuroprotective agent

Subject of

Numerous studies

Field of interest

Medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 3736-31-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,3 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3736-31:
(6*3)+(5*7)+(4*3)+(3*6)+(2*3)+(1*1)=90
90 % 10 = 0
So 3736-31-0 is a valid CAS Registry Number.

3736-31-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-1-propan-2-yl-2,3-dihydroindole-5,6-dione

1.2 Other means of identification

Product number -
Other names isoprenochrome

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:3736-31-0 SDS

3736-31-0Downstream Products

3736-31-0Relevant academic research and scientific papers

Photoproducts and proposed degradation pathway in the riboflavin-sensitised photooxidation of isoproterenol

Massad, Walter A.,Marioli,Garcia, Norman A.

, p. 1019 - 1021 (2007/10/03)

Products of the aerobic visible-light-promoted riboflavin-sensitised photooxidation of the sympathomimetic drug isoproterenol were identified by means of HPLC and spectrophotometric techniques. The oxidative process, mediated by superoxide radical anion, generates N-isopropylaminochrome as a main photoproduct with a quantum yield of 0.15. In parallel, the photodecomposition of riboflavin is prevented in the presence of isoproterenol. A reaction scheme for the photooxidation pathway of isoproterenol is proposed in analogy to former reports for related compounds.

MUSHROOM TYROSINASE AS AN OXIDANT FOR THE SYNTHESIS OF 5,6-DIHYDROXYINDOLE DERIVATIVES

Lim, Mu-Ill,Patil, Dilip G.

, p. 3775 - 3778 (2007/10/02)

Several catecholamines have been converted to 5,6-diacetoxyindole derivatives by the use of mushroom tyrosinase as oxidant.

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