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2,3-Dihydro-1-(1-methylpropyl)-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55955-58-3

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55955-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55955-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,5 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55955-58:
(7*5)+(6*5)+(5*9)+(4*5)+(3*5)+(2*5)+(1*8)=163
163 % 10 = 3
So 55955-58-3 is a valid CAS Registry Number.

55955-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(sec-butyl)indoline

1.2 Other means of identification

Product number -
Other names 1-sec-butyl-2,3-dihydro-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:55955-58-3 SDS

55955-58-3Downstream Products

55955-58-3Relevant 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

supporting information, p. 1589 - 1594 (2015/10/06)

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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