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2-((E)-2-Dimethylamino-vinyl)-3-nitro-benzoic acid ethyl ester is a complex organic chemical compound with the molecular formula C12H14N2O5. It is characterized by a benzoic acid structure, with a 3-nitro group and a 2-((E)-2-dimethylamino-vinyl) group attached to it. The ethyl ester functional group is present, indicating that the carboxylic acid group of the benzoic acid is esterified with ethanol. 2-((E)-2-Dimethylamino-vinyl)-3-nitro-benzoic acid ethyl ester is known for its potential applications in the synthesis of pharmaceuticals and as an intermediate in chemical reactions. It is important to handle 2-((E)-2-Dimethylamino-vinyl)-3-nitro-benzoic acid ethyl ester with care due to its reactivity and potential hazards associated with nitro and ester groups.

71516-34-2

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71516-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71516-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,1 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71516-34:
(7*7)+(6*1)+(5*5)+(4*1)+(3*6)+(2*3)+(1*4)=112
112 % 10 = 2
So 71516-34-2 is a valid CAS Registry Number.

71516-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(2-(dimethylamino)vinyl)-3-nitrobenzoate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:71516-34-2 SDS

71516-34-2Relevant academic research and scientific papers

A total synthesis of (±)-α-cyclopiazonic acid using a cationic cascade as a key step

Griffiths-Jones, Charlotte M.,Knight, David W.

, p. 8515 - 8528 (2011)

The indole alkaloid α-cyclopiazonic acid 1 has been synthesised by a route, which features at its core an acid-catalysed cationic cascade cyclisation terminated by a sulfonamide group.

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