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41710-89-8

2-Tetradecyloxyaniline is a chemical compound with the CAS Registry Number (69910-42-1). It is an organic compound that is primarily used for research or laboratory purposes in various scientific and biological fields. 2-Tetradecyloxyaniline has a creamy white to slightly yellow appearance. Although it is widely used for technical purposes, there is limited information available about its properties and potential effects on human health or the environment. It is important to handle this chemical with proper protective equipment and in a controlled environment as per the guidelines suggested by world health and chemical organizations.

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  • 41710-89-8 Structure

  • Basic information

    1. Product Name: 2-Tetradecyloxyaniline
    2. Synonyms: 2-TETRADECYLOXYANILINE;o-Tetradecyloxyaniline;2-(tetradecyloxy)benzenamine
    3. CAS NO:41710-89-8
    4. Molecular Formula: C20H35NO
    5. Molecular Weight: 305.5
    6. EINECS: 255-510-8
    7. Product Categories: N/A
    8. Mol File: 41710-89-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 420.5 °C at 760 mmHg
    3. Flash Point: 187.6 °C
    4. Appearance: /
    5. Density: 0.924 g/cm3
    6. Vapor Pressure: 2.8E-07mmHg at 25°C
    7. Refractive Index: 1.501
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-Tetradecyloxyaniline(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Tetradecyloxyaniline(41710-89-8)
    12. EPA Substance Registry System: 2-Tetradecyloxyaniline(41710-89-8)

  • 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: 41710-89-8(Hazardous Substances Data)

41710-89-8 Usage

Uses

Used in Scientific Research:
2-Tetradecyloxyaniline is used as a research compound for various scientific studies and experiments. It is employed in the development and testing of new materials, processes, and technologies in the fields of chemistry, biology, and materials science.
Used in Biological Studies:
In the field of biology, 2-Tetradecyloxyaniline is used as a reagent in various laboratory tests and assays. It aids in the investigation of biological processes and mechanisms, contributing to a better understanding of living organisms and their interactions.
Used in Material Development:
2-Tetradecyloxyaniline is used as a component in the synthesis of new materials with potential applications in various industries. Its unique chemical properties make it a valuable resource in the development of innovative products and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 41710-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,1 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41710-89:
(7*4)+(6*1)+(5*7)+(4*1)+(3*0)+(2*8)+(1*9)=98
98 % 10 = 8
So 41710-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H35NO/c1-2-3-4-5-6-7-8-9-10-11-12-15-18-22-20-17-14-13-16-19(20)21/h13-14,16-17H,2-12,15,18,21H2,1H3

41710-89-8Relevant articles and documents

Synthesis and biological evaluation of novel N-(alkoxyphenyl)-aminocarbonylbenzoic acid derivatives as PTP1B inhibitors

Tong, Yuan Feng,Zhang, Pei,Chen, Feng,Hao, Ling Hua,Ye, Fei,Tian, Jin Ying,Wu, Song

, p. 1415 - 1418 (2011/10/09)

Based on the fact that petroselinic acid showed good inhibitory activity (IC50=6.99μmol/L) against protein tyrosine phophatase 1B(PTP1B) in vitro, a series of novel N-(alkoxyphenyl)-aminocarbonylbenzoic acid derivatives were designed and synthesized. The results indicated that most of the derivatives showed more potent activities against PTP1B. Especially, compound 13 had obvious activity with an IC50 of 106nmol/L in vitro.

Method of producing aromatic amine derivatives

-

, (2008/06/13)

Disclosed is a method for producing aromatic amine derivatives in a high yield at a low price, which comprises inducing an aromatic hydroxamic acid derivative to undergo a rearrangement reaction under a mild condition in the presence of a base and a nitrile or a nitrile equivalent.

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