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5379-88-4

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5379-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5379-88-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,7 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5379-88:
(6*5)+(5*3)+(4*7)+(3*9)+(2*8)+(1*8)=124
124 % 10 = 4
So 5379-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H16N2O/c1-2-4-13-12(3-1)11(9-14-13)10-15-5-7-16-8-6-15/h1-4,9,14H,5-8,10H2

5379-88-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H63366)  3-(4-Morpholinylmethyl)indole, 95%   

  • 5379-88-4

  • 250mg

  • 784.0CNY

  • Detail
  • Alfa Aesar

  • (H63366)  3-(4-Morpholinylmethyl)indole, 95%   

  • 5379-88-4

  • 1g

  • 1882.0CNY

  • Detail
  • Alfa Aesar

  • (H63366)  3-(4-Morpholinylmethyl)indole, 95%   

  • 5379-88-4

  • 5g

  • 7840.0CNY

  • Detail

5379-88-4SDS

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 4-(1H-indol-3-ylmethyl)morpholine

1.2 Other means of identification

Product number -
Other names 3-Morpholinomethyl-indol

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:5379-88-4 SDS

5379-88-4Downstream Products

5379-88-4Relevant articles and documents

Bioactivity-guided synthesis of gramine derivatives as new MT1 and 5-HT1A receptors agonists

Yin, Xiu-Juan,Huang, Xiao-Yan,Ma, Yun-Bao,Geng, Chang-An,Li, Tian-Ze,Chen, Xing-Long,Yang, Tong-Hua,Zhou, Jun,Zhang, Xue-Mei,Chen, Ji-Jun

, p. 610 - 622 (2017/05/26)

Twenty-four gramine derivatives were synthesized and evaluated on MT1 and 5-HT1A receptors in vitro. Among them, seven derivatives (7, 8, 16, 19, 20, 21, and 24) exhibited higher agonisting activities on MT1 or 5-HT1A

12-Tungstophosphoric acid immobilized on γ-Fe2O 3@SiO2 coreshell nanoparticles: An effective solid acid catalyst for the synthesis of indole derivatives in water

Rafiee, Ezzat,Eavani, Sara,Malaekeh-Nikouei, Bizhan

scheme or table, p. 438 - 440 (2012/06/01)

12-Tungstophosphoric acid immobilized on γ-Fe2O 3@SiO2 coreshell nanoparticles was used as novel solid acid catalyst for the synthesis of various bis(indolyl)methanes and β-functionalized indoles in water. The catalyst can

Ruthenium-catalyzed /V-alkylation of amines and sulfonamides using borrowing hydrogen methodology

Hamid, M. Haniti S. A.,Allen, C. Liana,Lamb, Gareth W.,Maxwell, Aoife C.,Maytum, Hannah C.,et al.

supporting information; experimental part, p. 1766 - 1774 (2009/07/25)

The alkylation of amines by alcohols has been achieved using 0.5 mol percent [Ru(p-cymene)CI2]2 with the bidentate phosphines dppf or DPEphos as the catalyst. Primary amines have been converted into secondary amines, and secondary amines into tertiary amines, including the syntheses of Piribedil, Tripelennamine, and Chlorpheniramine. A/-Heterocyclization reactions of primary amines are reported, as well as alkylation reactions of primary sulfonamides. Secondary alcohols requiremore forcing conditions than primary alcohols but are still effective a lkylating agents in the presence of this catalyst.

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