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ethyl 2-(quinolin-3-yl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33054-18-1

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33054-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33054-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,5 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33054-18:
(7*3)+(6*3)+(5*0)+(4*5)+(3*4)+(2*1)+(1*8)=81
81 % 10 = 1
So 33054-18-1 is a valid CAS Registry Number.

33054-18-1SDS

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 ethyl 2-quinolin-3-ylacetate

1.2 Other means of identification

Product number -
Other names quinolin-3-yl-acetic acid ethyl ester

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:33054-18-1 SDS

33054-18-1Downstream Products

33054-18-1Relevant academic research and scientific papers

Oxidative Cascade Reaction of N-Aryl-3-alkylideneazetidines and Carboxylic Acids: Access to Fused Pyridines

Cai, Wangshui,Wang, Shuang,Jalani, Hitesh B.,Wu, Junxian,Lu, Hongjian,Li, Guigen

supporting information, p. 3833 - 3837 (2018/07/25)

A versatile silver-promoted oxidative cascade reaction of N-aryl-3-alkylideneazetidines with carboxylic acids is reported, providing a very efficient pathway to functionalized fused pyridines. This method allows introduction of fused pyridine ring systems

Facile access to ring-fused aminals via direct α-amination of secondary amines with o-aminobenzaldehydes: Synthesis of vasicine, deoxyvasicine, deoxyvasicinone, mackinazolinone, and ruteacarpine

Richers, Matthew T.,Deb, Indubhusan,Platonova, Alena Yu.,Zhang, Chen,Seidel, Daniel

, p. 1730 - 1748 (2013/07/26)

Secondary amines undergo redox-neutral reactions with aminobenzaldehydes under conventional and microwave heating to furnish polycyclic aminals via amine α-amination/N-alkylation. This unique α-functionalization reaction proceeds without the involvement of transition metals or other additives. The resulting aminal products are precursors for various quinazolinone alkaloids and their analogues. Georg Thieme Verlag Stuttgart. New York.

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