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4-nitro-o-phenetidine is a chemical compound that belongs to the family of aniline compounds. It is characterized by its nitro group (NO2) and phenetidine (a type of aromatic amine) structure. 4-nitro-o-phenetidine has been largely used in scientific studies for its distinctive chemical properties. The presence of both nitro and phenetidine groups can make it highly reactive, and these properties can have diverse implications in contexts such as organic synthesis and pharmaceutical sciences. However, as with other nitro compounds and anilines, 4-nitro-o-phenetidine needs to be handled with appropriate safety measures due to its potential for toxicity and environmental harm.

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  • 16383-89-4 Structure
  • Basic information

    1. Product Name: 4-nitro-o-phenetidine
    2. Synonyms: 4-nitro-o-phenetidine;4-Nitro-o-phenetidine (NH2=1);2-Ethyoxy-4-nitroaniline;5-Nitro-2-amino-1-ethoxybenzene;Benzenamine, 2-ethoxy-4-nitro-;Einecs 240-431-3
    3. CAS NO:16383-89-4
    4. Molecular Formula: C8H10N2O3
    5. Molecular Weight: 182.1766
    6. EINECS: 240-431-3
    7. Product Categories: Anilines, Amides & Amines;Anisoles, Alkyloxy Compounds & Phenylacetates;Nitro Compounds
    8. Mol File: 16383-89-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 369.4 °C at 760 mmHg
    3. Flash Point: 177.2 °C
    4. Appearance: COA
    5. Density: 1.264 g/cm3
    6. Vapor Pressure: 1.19E-05mmHg at 25°C
    7. Refractive Index: 1.585
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-nitro-o-phenetidine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-nitro-o-phenetidine(16383-89-4)
    12. EPA Substance Registry System: 4-nitro-o-phenetidine(16383-89-4)
  • 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: 16383-89-4(Hazardous Substances Data)

16383-89-4 Usage

Uses

Used in Organic Synthesis:
4-nitro-o-phenetidine is used as a reagent for various organic synthesis processes due to its reactive nature. The presence of the nitro group and phenetidine structure allows for a wide range of chemical reactions, making it a valuable compound in the synthesis of other organic compounds.
Used in Pharmaceutical Sciences:
4-nitro-o-phenetidine is used as a research tool in pharmaceutical sciences. Its unique chemical properties can be exploited to develop new drug candidates or to study the interactions of drugs with biological systems. The reactivity of the compound can also be utilized to investigate the mechanisms of drug action and to design more effective therapeutic agents.
Used in Scientific Studies:
4-nitro-o-phenetidine is used as a model compound in scientific studies to understand the behavior of nitro compounds and anilines. 4-nitro-o-phenetidine's reactivity and potential toxicity provide valuable insights into the chemical properties and safety considerations of similar compounds, which can be crucial for the development of new materials and pharmaceuticals.
Used in Environmental Research:
4-nitro-o-phenetidine is used as a reference compound in environmental research to study the fate and transport of nitro compounds in the environment. Understanding the behavior of 4-nitro-o-phenetidine can help in assessing the environmental impact of similar compounds and in developing strategies for their safe handling and disposal.

Check Digit Verification of cas no

The CAS Registry Mumber 16383-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,8 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16383-89:
(7*1)+(6*6)+(5*3)+(4*8)+(3*3)+(2*8)+(1*9)=124
124 % 10 = 4
So 16383-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O3/c1-2-13-8-5-6(10(11)12)3-4-7(8)9/h3-5H,2,9H2,1H3

16383-89-4SDS

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-ethoxy-4-nitroaniline

1.2 Other means of identification

Product number -
Other names 4-Nitro-o-phenetidin

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:16383-89-4 SDS

16383-89-4Relevant articles and documents

PH triggered smart organogel from DCDHF-Hydrazone molecular switch

Khattab, Tawfik A.,Tiu, Brylee David B.,Adas, Sonya,Bunge, Scott D.,Advincula, Rigoberto C.

, p. 327 - 336 (2016)

The design, synthesis and photophysical properties of a Low Molecular Weight pH-responsive Gelator (LMWG) based on alkoxy group functionalized DCDHF-Hydrazones (DCDHF-H) are described. A straightforward synthesis of DCDHF-Hydrazone (DCDHF-H) chromophores was achieved via simple azo-coupling starting from 2-(dicyanomethylene)-2,5-dihydro-4,5,5-trimethylfuran-3-carbonitrile and alkoxy bearing aryl diazonium chloride derivatives. The DCDHF-H efficiently gelate selected organic solvents and reversibly respond to pH stimuli with a gel-sol conversion and an associated color change from yellow to purple. Self-assembly of these molecules, as indicated by X-ray crystallography, occurs via cooperative π-π stacking and van der Waals interactions producing gelation in some pure and mixed organic solvents. Furthermore, the presence of acidic or alkaline gases leads to a dramatic change in the rheological properties with potential applications in areas such as gas detection devices and drug release systems. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) studies of the xerogels obtained from n-propanol provide visual images revealing the formation of fibrous nanostructures.

Amide compound and derivative thereof, preparation method, pharmaceutical composition and application thereof

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Paragraph 0470-0473, (2021/07/09)

The invention discloses an amide compound and derivative thereof, a preparation method, a pharmaceutical composition and application thereof. The structure of the amide compound is shown as a formula (I). The derivatives of theamide compound relate to a stereoisomer, a tautomer, a metabolite, a metabolic precursor, a prodrug, a solvate, a salt of the solvate, a crystal, a pharmaceutically acceptable salt or a mixture of the above of theamide compound. The amide compound and the derivative thereof have an efficient inhibition effect on indoleamine 2, 3-dioxygenase 1, and can be used for preparing medicines for treating indoleamine 2, 3-dioxygenase 1 mediated immunosuppression related diseases, the prepared medicine can exert the medicine effect at the molecular level and is wide in application, and the synthesis method of the compound is simple, convenient and easy to operate.

An attempt to modify nonlinear optical effects of polyurethanes by adjusting the structure of the chromophore moieties at the molecular level using "click" chemistry

Li, Zhong'an,Zeng, Qi,Li, Zhen,Dong, Shoucheng,Zhu, Zhichao,Li, Qianqian,Ye, Cheng,Di, Chong'an,Liu, Yunqi,Qin, Jingui

, p. 8544 - 8546 (2007/10/03)

The modification of the nonlinear optical effects (NLO) properties of polyurethanes by adjusting the structure of chromophore moieties at the molecular level by introducing different size of isolation spacers, was illustrated. One of the major problems arising while optimizing organic NLO materials is to efficiently translate the large β values of the organic chromophores into high macroscopic NLO activities of polymers. The isolation parts in the chromophore moieties can weaken the strong intermolecular electrostatic interaction to enhance the resultant macroscopic NLO effect of polymers. The dynamic thermal stabilities of the NLO activities of the polymers are investigated by depoling experiments where the real time decays of their SHG signals are monitored. The results show that the NLO properties do not always increase accompanying with the entanglement of the isolation groups linked to the corresponding chromophore moieties.

A convenient method to aniline compounds using microwave-assisted transfer hydrogenation

Chapman, Nicholas,Conway, Benjamin,O'Grady, Fiona,Wall, Michael D.

, p. 1043 - 1046 (2007/10/03)

The reduction of mononitro and dinitro aromatic compounds to their aniline analogues using microwave-assisted transfer hydrogenation has been demonstrated. The optimised conditions used, with some examples, are described herein. Georg Thieme Verlag Stuttgart.

Quinone Imine Route to Benzimidazol-2-ylcarbamates. Part 3. Effect of Extension of Conjugation in the Quinone Imine.

Divakar, Kikkeri J.,Gaikwad Balkrishna V.,Tampal, Nilufer F.,Rajappa, Srinivasachari

, p. 1687 - 1697 (2007/10/02)

5-Aminobenzimidazol-2-ylcarbamates (11) and (17), in which the amine is linked to position 3 of 1,2-benzisothiazole 1,1-dioxide have been synthesised in good yields from the guanidines (10) and (16) by oxidative cyclisation.The cyclisation is regiospecific.It is likely that quinone imines with extended conjugation are intermediates in this reaction.

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