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2,4-Pentadienoic acid, 2-azido-5,5-diphenyl-, methyl ester is a chemical compound with the molecular formula C17H15N3O2. It is a methyl ester derivative of 2-azido-5,5-diphenyl-2,4-pentadienoic acid, featuring a unique azido group and a conjugated dienoic acid structure. 2,4-Pentadienoic acid, 2-azido-5,5-diphenyl-, methyl ester is utilized in various chemical processes and synthesis, making it a valuable reagent in the field of organic chemistry.

116340-87-5

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116340-87-5 Usage

Uses

Used in Organic Synthesis:
2,4-Pentadienoic acid, 2-azido-5,5-diphenyl-, methyl ester is used as a reagent in organic synthesis for various reactions. Its azido group and dienoic acid structure make it a versatile building block for the creation of complex molecules and compounds.
Used in Chemical Compound Preparation:
2,4-Pentadienoic acid, 2-azido-5,5-diphenyl-, methyl ester is also used in the preparation of other chemical compounds, where its unique structure and reactivity can be harnessed to produce desired products. Its role in the synthesis of new compounds highlights its importance in the development of novel materials and substances.
Used in Pharmaceutical Industry:
2,4-Pentadienoic acid, 2-azido-5,5-diphenyl-, methyl ester is used as a key intermediate in the synthesis of certain pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Research and Development:
In the field of research and development, 2,4-Pentadienoic acid, 2-azido-5,5-diphenyl-, methyl ester is used as a model compound to study the reactivity and properties of azido and dienoic acid groups. This helps in understanding the underlying chemical mechanisms and can lead to the discovery of new reaction pathways and applications.
Safety Precautions:
It is important to handle 2,4-Pentadienoic acid, 2-azido-5,5-diphenyl-, methyl ester with care, as it may be hazardous if not used properly. It can cause skin and eye irritation, and may also be harmful if inhaled or ingested. Proper safety measures, such as wearing protective clothing and using appropriate containment, should be taken to minimize the risk of exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 116340-87-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,3,4 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 116340-87:
(8*1)+(7*1)+(6*6)+(5*3)+(4*4)+(3*0)+(2*8)+(1*7)=105
105 % 10 = 5
So 116340-87-5 is a valid CAS Registry Number.

116340-87-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-azido-5,5-diphenylpenta-2,4-dienoate

1.2 Other means of identification

Product number -
Other names 2-Azido-5,5-diphenyl-2,4-pentadiensaeuremethylester

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:116340-87-5 SDS

116340-87-5Relevant academic research and scientific papers

Iron-Catalyzed Radical Activation Mechanism for Denitrogenative Rearrangement Over C(sp3)–H Amination

Roy, Satyajit,Das, Sandip Kumar,Khatua, Hillol,Das, Subrata,Singh, Krishna Nand,Chattopadhyay, Buddhadeb

supporting information, p. 8772 - 8780 (2021/03/16)

An iron-catalyzed denitrogenative rearrangement of 1,2,3,4-tetrazole is developed over the competitive C(sp3)–H amination. This catalytic rearrangement reaction follows an unprecedented metalloradical activation mechanism. Employing the developed method, a wide number of complex-N-heterocyclic product classes have been accessed. The synthetic utility of this radical activation method is showcased with the short synthesis of a bioactive molecule. Collectively, this discovery underlines the progress of radical activation strategy that should find wide application in the perspective of medicinal chemistry, drug discovery and natural product synthesis research.

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