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4-NITROPHENYL ANTHRANILATE is a chemical compound that features a nitrophenyl group connected to an anthranilate moiety. It is recognized for its capacity to absorb ultraviolet (UV) radiation, which makes it a valuable component in various applications, particularly in the realm of cosmetics and pharmaceuticals.

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  • 19176-60-4 Structure
  • Basic information

    1. Product Name: 4-NITROPHENYL ANTHRANILATE
    2. Synonyms: ANTHRANILIC ACID 4-NITROPHENYL ESTER;4-NITROPHENYL ANTHRANILATE;2-AMINOBENZOIC ACID 4-NITROPHENYL ESTER;4-Nitrophenyl 2-aminobenzoate;Anthralinic acid 4-Nitrophenyl ester;Anthanilic acid 4-nitrophenyl ester;Anthanilic acid p-nitrophenyl ester;o-Aminobenzoic acid p-nitrophenyl ester
    3. CAS NO:19176-60-4
    4. Molecular Formula: C13H10N2O4
    5. Molecular Weight: 258.23
    6. EINECS: N/A
    7. Product Categories: Phenyl Esters (Liquid Crystals);Functional Materials;Liquid Crystals & Related Compounds
    8. Mol File: 19176-60-4.mol
  • Chemical Properties

    1. Melting Point: 127-129°C
    2. Boiling Point: 467 °C at 760 mmHg
    3. Flash Point: 236.2 °C
    4. Appearance: yellow/crystalline
    5. Density: 1.381 g/cm3
    6. Refractive Index: 1.656
    7. Storage Temp.: N/A
    8. Solubility: almost transparency in hot Methanol
    9. PKA: 1.89±0.10(Predicted)
    10. CAS DataBase Reference: 4-NITROPHENYL ANTHRANILATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-NITROPHENYL ANTHRANILATE(19176-60-4)
    12. EPA Substance Registry System: 4-NITROPHENYL ANTHRANILATE(19176-60-4)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 19176-60-4(Hazardous Substances Data)

19176-60-4 Usage

Uses

Used in Cosmetics Industry:
4-NITROPHENYL ANTHRANILATE is used as a UV-absorbing agent for its ability to absorb UV radiation, thereby providing protection to the skin from harmful sun exposure. This application is particularly relevant in the formulation of sunscreen and other cosmetic products designed to shield the skin from the damaging effects of UV rays.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 4-NITROPHENYL ANTHRANILATE serves as a precursor in the synthesis of an array of drugs and active pharmaceutical ingredients. Its role in drug development capitalizes on its unique chemical properties, which can be harnessed to create new therapeutic agents.
Used in Organic Synthesis and Material Science:
4-NITROPHENYL ANTHRANILATE also finds potential applications in the fields of organic synthesis and material science. Its distinctive chemical characteristics allow it to be utilized in the development of new materials and compounds, contributing to advancements in these scientific domains.
It is crucial to handle 4-NITROPHENYL ANTHRANILATE with care, adhering to proper safety measures and storage guidelines to mitigate any potential risks it may pose to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 19176-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,7 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19176-60:
(7*1)+(6*9)+(5*1)+(4*7)+(3*6)+(2*6)+(1*0)=124
124 % 10 = 4
So 19176-60-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2O4/c14-11-8-10(15(17)18)6-7-12(11)19-13(16)9-4-2-1-3-5-9/h1-8H,14H2

19176-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-nitrophenyl) 2-aminobenzoate

1.2 Other means of identification

Product number -
Other names 2-Aminobenzoic Acid 4-Nitrophenyl 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:19176-60-4 SDS

19176-60-4Relevant articles and documents

Thermo-Promoted Reactions of Anthranils with Carboxylic Acids, Amines, Phenols, and Malononitrile under Catalyst-Free Conditions

Jiang, Jing,Cai, Xin,Hu, Yanwei,Liu, Xuejun,Chen, Xiaodong,Wang, Shun-Yi,Zhang, Yinan,Zhang, Shilei

supporting information, p. 2022 - 2031 (2019/05/16)

A convenient and atom-economical procedure for the thermo-promoted reactions of anthranil with different substrates was developed. The catalyst-free process affords various useful building blocks with good to moderate yields. This chemistry enables several step- and cost-effective approaches for biologically interesting molecules and provides an efficient platform for the investigation of untapped reactions at high temperature.

Investigations on preparation and reactivity of c-anellated derivatives of 1, 3, 4-benzotriazepines and related precursors N, N-coupled heterobicycles from cyclic hydrazine derivatives, part 12

Morgenstern,Schuster,Finke,Richter

, p. 458 - 467 (2007/10/03)

c-Anellated 1, 3, 4-benzotriazepines are hitherto unknown. In order to synthesize derivatives of pyrazolo[l, 2-c]- and phthalazino[2, 3-c][l, 3, 4]benzotriazepines the intramolecular cyclization of N-(N-arylthiocarbamoyl)-pyrazolidines and -1, 2, 3, 4-tet

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