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

52604-06-5

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52604-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52604-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,0 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52604-06:
(7*5)+(6*2)+(5*6)+(4*0)+(3*4)+(2*0)+(1*6)=95
95 % 10 = 5
So 52604-06-5 is a valid CAS Registry Number.

52604-06-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hexyl-1H-indole

1.2 Other means of identification

Product number -
Other names 1H-Indole,3-hexyl

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:52604-06-5 SDS

52604-06-5Downstream Products

52604-06-5Relevant academic research and scientific papers

Ruthenium Pincer Complex Catalyzed Selective Synthesis of C-3 Alkylated Indoles and Bisindolylmethanes Directly from Indoles and Alcohols

Biswas, Nandita,Sharma, Rahul,Srimani, Dipankar

supporting information, p. 2902 - 2910 (2020/06/03)

Herein, we presented Ru-SNS complex that serves as a useful catalyst for C-3 alkylation of 1H-indoles with various aliphatic primary and secondary alcohols including cyclic alcohols as well as benzylic alcohols. The selective synthesis of bisindolylmethane derivatives is also achieved from the same set of indole and alcohol just by altering the reaction parameters. Furthermore, the sustainable synthesis of C-3 alkylated indoles directly from 2-(2-nitrophenyl)ethan-1-ol and alcohols catalysed by a Ru-complex via “borrowing hydrogen” strategy is reported. This protocol provides an atom-economical sustainable route to access structurally important compounds like arundine, vibrindole A and tryptamine based derivatives. (Figure presented.).

Selective ruthenium-catalyzed alkylation of indoles by using amines

Imm, Sebastian,Baehn, Sebastian,Tillack, Annegret,Mevius, Kathleen,Neubert, Lorenz,Beller, Matthias

supporting information; scheme or table, p. 2705 - 2709 (2010/06/16)

(Chemical Equation Presented) Lend me your hydrogen! The first transition-metal-catalyzed alkylations of indoles with aliphatic amines proceeding under transfer hydrogenation conditions are developed (see scheme). This reaction is based on the borrowing h

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