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61312-59-2

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61312-59-2 Usage

Description

Isobutyl 2-(2-Nitro-Benzylidene)Acetoacetate, with the chemical name 2-(2-nitrobenzylidene)-1,1-dimethylethyl 3-oxobutanoate and CAS number 61312-59-2, is an organic compound that serves as an important intermediate in the synthesis of various organic compounds. Its unique structure, featuring a nitro group and a benzylidene moiety, allows it to participate in a range of chemical reactions, making it a valuable building block in organic chemistry.

Uses

Used in Organic Synthesis:
Isobutyl 2-(2-Nitro-Benzylidene)Acetoacetate is used as a key intermediate in the synthesis of various organic compounds for different applications. Its reactivity and functional groups enable it to undergo a variety of chemical transformations, such as reduction, hydrolysis, and condensation reactions, which can lead to the formation of a wide range of products.
Used in Pharmaceutical Industry:
Isobutyl 2-(2-Nitro-Benzylidene)Acetoacetate is used as a starting material or intermediate in the synthesis of pharmaceutical compounds. Its unique structure can be modified to create new drug candidates with potential therapeutic properties. Isobutyl 2-(2-Nitro-Benzylidene)Acetoacetate's versatility in organic synthesis allows for the development of novel drug molecules with improved pharmacokinetic and pharmacodynamic profiles.
Used in Chemical Research:
Isobutyl 2-(2-Nitro-Benzylidene)Acetoacetate is used as a research tool in chemical laboratories to study various reaction mechanisms and explore new synthetic pathways. Its reactivity and structural features make it an ideal candidate for investigating new chemical reactions and understanding the underlying principles of organic chemistry.
Used in Material Science:
Isobutyl 2-(2-Nitro-Benzylidene)Acetoacetate can be used in the development of new materials with specific properties, such as polymers, dyes, and sensors. Its ability to undergo various chemical reactions allows for the creation of materials with tailored characteristics, making it a valuable component in material science research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 61312-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,1 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61312-59:
(7*6)+(6*1)+(5*3)+(4*1)+(3*2)+(2*5)+(1*9)=92
92 % 10 = 2
So 61312-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H17NO5/c1-10(2)9-21-15(18)13(11(3)17)8-12-6-4-5-7-14(12)16(19)20/h4-8,10H,9H2,1-3H3

61312-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylpropyl 2-[(2-nitrophenyl)methylidene]-3-oxobutanoate

1.2 Other means of identification

Product number -
Other names Butanoic acid,2-[(2-nitrophenyl)methylene]-3-oxo-,2-methylpropyl 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:61312-59-2 SDS

61312-59-2Relevant articles and documents

An efficient and recyclable 3D printed α-Al2O3 catalyst for the multicomponent assembly of bioactive heterocycles

Azuaje, Jhonny,Tubío, Carmen R.,Escalante, Luz,Gómez, Mónica,Guitián, Francisco,Coelho, Alberto,Caama?o, Olga,Gil, Alvaro,Sotelo, Eddy

, p. 203 - 210 (2016/12/09)

A catalytic methodology is reported that enables the efficient, operationally simple and environmentally friendly synthesis of diverse 1,4-dihydropyridines and 3,4-dihydropyrimidin-2(1H)-ones, including some relevant drugs and pharmacologically active derivatives. This strategy is based on the use of a 3D printed Al2O3 woodpile material that was sintered to generate a rigid structure with controlled porosity and noteworthy catalytic performance. The 3D printed Al2O3 catalyst exhibits remarkable efficacy as a Lewis acid in Biginelli and Hantzsch reactions and it can be recovered and reused ten times without any decrease in the activity. Remarkable E factors, excellent recyclability and scalability, broad substrate scope, short reaction times, excellent yields, solvent-free conditions and easy isolation procedures are key features of this methodology.

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