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53560-33-1

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53560-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53560-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,6 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53560-33:
(7*5)+(6*3)+(5*5)+(4*6)+(3*0)+(2*3)+(1*3)=111
111 % 10 = 1
So 53560-33-1 is a valid CAS Registry Number.

53560-33-1SDS

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 5-ethynyl-1,2,3-trimethoxybenzene

1.2 Other means of identification

Product number -
Other names Benzene,5-ethynyl-1,2,3-trimethoxy

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:53560-33-1 SDS

53560-33-1Relevant articles and documents

Synthesis and biological evaluation of 1-(benzofuran-3-yl)-4-(3,4,5-trimethoxyphenyl)-1H-1,2,3-triazole derivatives as tubulin polymerization inhibitors

Qi, Zhi-Yuan,Hao, Shu-Yi,Tian, Heng-Zhi,Bian, Hong-Li,Hui, Ling,Chen, Shi-Wu

, (2020)

The key functions of microtubules and the mitotic spindle in cell division make them attractive targets for cancer therapy. In this study, a series of 1-(benzofuran-3-yl)-4-(3,4,5-trimethoxyphenyl)-1H-1,2,3-triazole derivatives was synthesized, and their

De Novo Synthesis of Tricyclic 5,5-Benzannulated Spiroketals

Rao, Maddali L. N.,Islam, Sk Shamim

, p. 3944 - 3948 (2021/05/29)

The synthesis of tricyclic 5,5-benzannulated spiroketal scaffolds was accomplished from 2′-hydroxyacetophenones and gem-dibromoalkenes involving a one-pot domino strategy. The hitherto unknown transformation afforded the tricyclic 5,5-benzannulated spirok

Copper-catalyzed domino synthesis of ynamines

Dasgupta, Priyabrata,Islam, Sk Shamim,Rao, Maddali L. N.

, p. 7855 - 7860 (2021/09/28)

The hitherto unexploredN-alkynylation of electron-withdrawing or protecting group free N-heteroarenes such as indole, carbazole and pyrrole was developed usinggem-dibromoalkenes to synthesize ynamines under ligand-free copper-catalyzed domino conditions. The development methodology of ynamines was also applied in the synthesis of enynamines, multi-coupled bis-ynamines, tris-ynamines, and the natural product peyonine, demonstrating its broad synthetic scope and applications.

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