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

67765-91-7

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67765-91-7 Usage

Indole derivative

A chemical compound that is a modified version of the indole structure.

Synthesis of pharmaceuticals and agrochemicals

Used as a building block or intermediate in the production of drugs and pesticides.

Strong odor

Has a noticeable and intense smell.

Scent of jasmine and orange blossoms

Can be found as a component in the fragrances of these flowers.

Natural component of certain essential oils

Occurs naturally in some essential oils extracted from plants.

Potential environmental contaminant

May cause pollution to the environment and is regulated by environmental protection agencies.

Potential health effects

Studies have found that it may have harmful effects on human health, including cytotoxic (cell-damaging) and genotoxic (DNA-damaging) properties.

Check Digit Verification of cas no

The CAS Registry Mumber 67765-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,6 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67765-91:
(7*6)+(6*7)+(5*7)+(4*6)+(3*5)+(2*9)+(1*1)=177
177 % 10 = 7
So 67765-91-7 is a valid CAS Registry Number.

67765-91-7SDS

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-butan-2-yl-1H-indole

1.2 Other means of identification

Product number -
Other names 3-sec-butyl-indole

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:67765-91-7 SDS

67765-91-7Downstream Products

67765-91-7Relevant academic research and scientific papers

Synthesis of N-Alkylated Indolines and Indoles from Indoline and Aliphatic Ketones

Bayindir, Sinan,Erdogan, Esra,Kilic, Haydar,Aydin, Omer,Saracoglu, Nurullah

, p. 1589 - 1594 (2015)

A survey of redox aminations of indoline with aliphatic ketones using bismuth nitrate as catalyst is described. A reaction of an equivalent amount of indoline and aliphatic cyclic and acyclic ketones provides a mixture of excessive alkylated indole derivatives over typically redox isomerization and reductive alkylation pathways while using of the five equivalent of indoline provides N-alkylated indolines as a reductive alkylation product. The desired N-alkyl indoles from the oxidation of N-alkyl indolines were obtained in excellent yields.

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