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1H-INDOLE,6-BROMO-3-(2-IODOETHYL)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

694439-91-3

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694439-91-3 Usage

Chemical Class

Indole compounds

Structure

Complex organic molecule with a bromine atom at the 6th position and an ethyl-iodide side chain at the 3rd position of the indole ring

Potential Applications

Medicinal chemistry, drug development, biological activity, synthesis of pharmaceuticals and research compounds

Precautions

Potential reactivity and toxicity, should be handled with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 694439-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,4,4,3 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 694439-91:
(8*6)+(7*9)+(6*4)+(5*4)+(4*3)+(3*9)+(2*9)+(1*1)=213
213 % 10 = 3
So 694439-91-3 is a valid CAS Registry Number.

694439-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-3-(2-iodoethyl)indole

1.2 Other means of identification

Product number -
Other names 1H-INDOLE,6-BROMO-3-(2-IODOETHYL)-

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:694439-91-3 SDS

694439-91-3Downstream Products

694439-91-3Relevant academic research and scientific papers

Total Synthesis of (±)-Perophoramidine

Fuchs, James R.,Funk, Raymond L.

, p. 5068 - 5069 (2004)

The first total synthesis of racemic perophoramidine is described. The key step features the highly stereoselective introduction of the vicinial quaternary centers via base-promoted carbon-carbon bond formation between a 3-alkylindole and a 3-bromo-3-alkylindolin-2-one. This transformation presumably proceeds through a conjugate addition or Diels-Alder cycloaddition of the 3-alkylindole with a 3-alkylindol-2-one intermediate. Copyright

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