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Dimethyl [2-(2-nitrophenyl)ethyl]propanedioate is a complex organic compound with the chemical formula C13H15NO6. It is a derivative of propanedioic acid, featuring a dimethyl ester group and a 2-nitrophenylethyl substituent. dimethyl [2-(2-nitrophenyl)ethyl]propanedioate is characterized by its nitro group attached to the phenyl ring, which imparts specific chemical properties and reactivity. It is used in various chemical synthesis processes, particularly in the production of pharmaceuticals and other specialty chemicals. Due to its complex structure, it is typically synthesized through multi-step reactions and is not found naturally. The compound's properties, such as its solubility and stability, can be influenced by the presence of the nitro group and the ester functionality, making it a versatile building block in organic chemistry.

5395-45-9

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5395-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5395-45-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5395-45:
(6*5)+(5*3)+(4*9)+(3*5)+(2*4)+(1*5)=109
109 % 10 = 9
So 5395-45-9 is a valid CAS Registry Number.

5395-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-[2-(2-nitrophenyl)ethyl]propanedioate

1.2 Other means of identification

Product number -
Other names dimethyl[2-(2-nitrophenyl)ethyl]propanedioate

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 -
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More Details:5395-45-9 SDS

5395-45-9Downstream Products

5395-45-9Relevant academic research and scientific papers

Intramolecular Pd-catalyzed reductive amination of enolizable sp3-C-H bonds

Ford, Russell L.,Alt, Isabel,Jana, Navendu,Driver, Tom G.

supporting information, p. 8827 - 8831 (2019/10/28)

A palladium-catalyzed reductive cyclization of nitroarenes has been designed to construct sp3-C-NHAr bonds from sp3-C-H bonds by using an enolizable nucleophile to intercept a nitrosoarene intermediate. Exposure of ortho-substituted nitroarenes to 5 mol ?% of Pd(OAc)2 and 10 mol ?% of phenanthroline under 2 atm of CO constructs partially saturated 5-, 6-, or 7-membered N-heterocycles using α-pyridyl carboxylates, malonates, 1,3-dimethylbarbituric acid, 1,3-diones, or difurans as the nucleophile.

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