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CAS

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122329-02-6

2-Tetradecyloxynitrobenzene, also known as 1-Nitro-2-(tetradecyloxy)benzene, is an organic compound with the molecular formula C20H31NO3. It is characterized by a nitro group attached to a benzene ring and a tetradecyloxy group, which is a long alkyl chain with 14 carbon atoms. 2-Tetradecyloxynitrobenzene has potential applications in various fields due to its unique chemical structure and properties.

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  • 122329-02-6 Structure

  • Basic information

    1. Product Name: 2-Tetradecyloxynitrobenzene
    2. Synonyms: O-Tetradecyloxynitro-Benzene;2-NITROPHENYLTETRADECYLETHER;2-Tetradecyloxynitrobenzene;1-Nitro-2-(tetradecyloxy)benzene
    3. CAS NO:122329-02-6
    4. Molecular Formula: C20H33NO3
    5. Molecular Weight: 335.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122329-02-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 443.4 °C at 760 mmHg
    3. Flash Point: 149.3 °C
    4. Appearance: /
    5. Density: 0.987 g/cm3
    6. Vapor Pressure: 1.21E-07mmHg at 25°C
    7. Refractive Index: 1.498
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-Tetradecyloxynitrobenzene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Tetradecyloxynitrobenzene(122329-02-6)
    12. EPA Substance Registry System: 2-Tetradecyloxynitrobenzene(122329-02-6)

  • 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: 122329-02-6(Hazardous Substances Data)

122329-02-6 Usage

Uses

Used in Pharmaceutical Industry:
2-Tetradecyloxynitrobenzene is used as a protein tyrosine phosphatase 1B (PTP1B) inhibitor for the development of drugs targeting type 2 diabetes and obesity. PTP1B is an enzyme that negatively regulates insulin signaling, and its inhibition can help improve insulin sensitivity and glucose homeostasis. By acting as a PTP1B inhibitor, 2-Tetradecyloxynitrobenzene can potentially contribute to the treatment of metabolic disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 122329-02-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,3,2 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 122329-02:
(8*1)+(7*2)+(6*2)+(5*3)+(4*2)+(3*9)+(2*0)+(1*2)=86
86 % 10 = 6
So 122329-02-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H33NO3/c1-2-3-4-5-6-7-8-9-10-11-12-15-18-24-20-17-14-13-16-19(20)21(22)23/h13-14,16-17H,2-12,15,18H2,1H3

122329-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-nitro-2-tetradecoxybenzene

1.2 Other means of identification

Product number -
Other names o-tetradecyloxynitrobenzene

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:122329-02-6 SDS

122329-02-6Relevant 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

scheme or table, 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.

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