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1H-Indole-3-ethanol, acetate (ester) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13137-14-9

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13137-14-9 Usage

Derivation

Derived from indole, a natural compound found in some flowers and plants

Uses

Commonly used in the production of perfumes and fragrances, manufacturing of flavorings, as a chemical intermediate in the synthesis of pharmaceuticals and other organic compounds

Scent

Often used to add a floral and fruity scent to various consumer products

Medicinal properties

Has been studied for its potential anti-inflammatory and antioxidant effects

Industries

Versatile and valuable chemical used in various industries, including the perfume, flavoring, and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 13137-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,3 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13137-14:
(7*1)+(6*3)+(5*1)+(4*3)+(3*7)+(2*1)+(1*4)=69
69 % 10 = 9
So 13137-14-9 is a valid CAS Registry Number.

13137-14-9SDS

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 tryptophol acetate

1.2 Other means of identification

Product number -
Other names 1-acetoxy-2-indol-3-yl-ethane

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:13137-14-9 SDS

13137-14-9Relevant academic research and scientific papers

Hydroformylation of 2-Alkynylanilines: Toward an Alternative Methodology for the Synthesis of 3-Substituted Indoles

Holzapfel, Cedric,Dasilva, Etelinda,Den Drijver, Laetitia,Bredenkamp, Tyler

, p. 2912 - 2915 (2016/09/28)

A potentially viable route for the synthesis of 3-substituted indoles is presented herein. The methodology is based on a regioselective Rh-catalysed hydroformylation of prepared 2-alkyn-1-ylanilines. The requisite 2-alkynylaniline substrates were prepared in high yields (>85 %) using the Pd-catalysed Sonogashira reaction. A catalyst complex that comprises RhI(CO)(PPh3)3 and 1,2-bis(diphenylphosphino)ethane as the ligand allowed the quantitative conversions of the alkynyl substrates with selectivities >75 % for the desired 3-substituted indoles.

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