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2,4-dinitrophenyl propanoate is a chemical compound characterized by its molecular formula C12H11NO6. It presents as a yellow to orange crystalline solid, which is widely recognized for its reactivity in chemical processes. 2,4-dinitrophenyl propanoate is frequently utilized in organic synthesis and is particularly notable for its role in the preparation of esters of β-lactams. Due to its potential hazards, it is crucial to handle 2,4-dinitrophenyl propanoate with care, typically within a controlled laboratory setting.

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  • 32113-35-2 Structure
  • Basic information

    1. Product Name: 2,4-dinitrophenyl propanoate
    2. Synonyms:
    3. CAS NO:32113-35-2
    4. Molecular Formula: C9H8N2O6
    5. Molecular Weight: 240.1696
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 32113-35-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 375.7°C at 760 mmHg
    3. Flash Point: 177.4°C
    4. Appearance: N/A
    5. Density: 1.435g/cm3
    6. Vapor Pressure: 7.62E-06mmHg at 25°C
    7. Refractive Index: 1.575
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,4-dinitrophenyl propanoate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,4-dinitrophenyl propanoate(32113-35-2)
    12. EPA Substance Registry System: 2,4-dinitrophenyl propanoate(32113-35-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 32113-35-2(Hazardous Substances Data)

32113-35-2 Usage

Uses

Used in Organic Synthesis:
2,4-dinitrophenyl propanoate is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, facilitating the formation of esters and contributing to the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,4-dinitrophenyl propanoate is used as a precursor in the preparation of esters of β-lactams, which are important components in the development of antibiotics and other medicinal compounds.
Used in Chemical Reactions:
2,4-dinitrophenyl propanoate is employed as a reagent in chemical reactions for its reactivity, particularly in the formation of esters, which is a key step in the synthesis of various organic compounds.
Used in Extraction Processes:
As a solvent, 2,4-dinitrophenyl propanoate is used in the extraction of organic compounds, where its properties allow for the efficient separation of substances from mixtures.

Check Digit Verification of cas no

The CAS Registry Mumber 32113-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,1 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32113-35:
(7*3)+(6*2)+(5*1)+(4*1)+(3*3)+(2*3)+(1*5)=62
62 % 10 = 2
So 32113-35-2 is a valid CAS Registry Number.

32113-35-2SDS

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 (2,4-dinitrophenyl) propanoate

1.2 Other means of identification

Product number -
Other names CPD-8878

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:32113-35-2 SDS

32113-35-2Relevant articles and documents

Volatility of some aromatic nitrosubstituted plasticizers for polymers

Golubev,Novikov,Kuvshinova,Burmistrov,Koifman

, p. 2188 - 2194 (2017/10/27)

Nine derivatives of nitrophthalic acids and nitrophenols were synthesized as potential plasticizers for polymers and structurally characterized by 1H NMR and elemental analysis. The time dependences of the weight loss for the nitro derivatives

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