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3802-81-1

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3802-81-1 Usage

Derived from

Indole, a heterocyclic aromatic organic compound

Main properties

1. Bioactivity: Potential bioactivity and pharmacological properties.
2. Applications:
Organic synthesis: Commonly used in organic synthesis.
Pharmaceutical research: Used in pharmaceutical research.
Drug development: Potential applications in developing new drugs.
Neuropharmacology and oncology: Potential applications in these fields.
3. Utility:
Building block: Can serve as a building block in synthesizing more complex chemical entities.

Check Digit Verification of cas no

The CAS Registry Mumber 3802-81-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,0 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3802-81:
(6*3)+(5*8)+(4*0)+(3*2)+(2*8)+(1*1)=81
81 % 10 = 1
So 3802-81-1 is a valid CAS Registry Number.

3802-81-1SDS

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 (6-fluoro-1H-indol-3-yl) acetate

1.2 Other means of identification

Product number -
Other names Essigsaeure-(6-fluor-indol-3-ylester)

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:3802-81-1 SDS

3802-81-1Downstream Products

3802-81-1Relevant articles and documents

A revised synthetic scheme of 6,6′-dibromoindirubin

Tanoue, Yasuhiro,Hara, Akari,Kai, Norihisa,Sakata, Kazunori,Hashimoto, Mamoru,Nagai, Takeshi

, p. 1135 - 1137 (2008/04/12)

(Chemical Equation Presented) The synthetic scheme of 6,6′- dibromoindirubin (2) was investigated in detail. The reaction of 6-fluoro-3-acetoxyindole (7) with isatin (8) in methanol with Na 2CO3 produced 6′-fluoroindirubin in moderate yields. Its structure determination was mainly undertaken using 1H NMR spectroscopy. On the basis of this result, the synthetic scheme of 2 reported by Cooksey was revised.

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