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Vibrindole A is a natural product derived from the Vibrio splendidus bacteria, which is known for its potential bioactivity. This chemical compound has garnered interest due to its unique structure and potential applications in the field of drug discovery. It exhibits a tricyclic core with a pyrrole ring fused to a cyclohexene ring, which is further connected to a pyridine ring. The molecule is characterized by the presence of a chlorine atom and a hydroxyl group, which contribute to its chemical properties. Research on Vibrindole A is still in its early stages, but it holds promise for future studies in antimicrobial, anticancer, or other therapeutic areas, as its bioactivity and mechanism of action are further explored.

5030-91-1

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5030-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5030-91-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,3 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5030-91:
(6*5)+(5*0)+(4*3)+(3*0)+(2*9)+(1*1)=61
61 % 10 = 1
So 5030-91-1 is a valid CAS Registry Number.

5030-91-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[1-(1H-indol-3-yl)ethyl]-1H-indole

1.2 Other means of identification

Product number -
Other names 1H-Indole,3,3'-ethylidenebis

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:5030-91-1 SDS

5030-91-1Downstream Products

5030-91-1Relevant academic research and scientific papers

One-pot synthesis of symmetric and unsymmetric 1,1-bis-indolylmethanes via tandem iron-catalyzed C-H bond oxidation and C-O bond cleavage

Guo, Xingwei,Pan, Shiguang,Liu, Jinhua,Li, Zhiping

supporting information; experimental part, p. 8848 - 8851 (2010/03/02)

(Chemical Equation Presented) The reactions of indoles with ethers give a variety of symmetric and unsymmetric 1,1-bis-indolylmethane derivatives via iron-catalyzed C-H bond oxidation and C-O bond cleavage. 2009 American Chemical Society.

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