Welcome to LookChem.com Sign In|Join Free

CAS

  • or
1-Nitro-4-(prop-2-yn-1-yloxy)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17061-85-7 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 17061-85-7 Structure
  • Basic information

    1. Product Name: 1-Nitro-4-(prop-2-yn-1-yloxy)benzene
    2. Synonyms: 1-Nitro-4-(prop-2-yn-1-yloxy)benzene;1-nitro-4-(2-propyn-1-yloxy)Benzene;1-NITRO-4-(2-PROPYNYLOXY)BENZENE
    3. CAS NO:17061-85-7
    4. Molecular Formula: C9H7NO3
    5. Molecular Weight: 177.15678
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17061-85-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Nitro-4-(prop-2-yn-1-yloxy)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Nitro-4-(prop-2-yn-1-yloxy)benzene(17061-85-7)
    11. EPA Substance Registry System: 1-Nitro-4-(prop-2-yn-1-yloxy)benzene(17061-85-7)
  • 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: 17061-85-7(Hazardous Substances Data)

17061-85-7 Usage

Nitroaromatic compound

A type of aromatic compound that contains a nitro group (-NO2) attached to a benzene ring.

Alkyne group

A carbon-carbon triple bond (C≡C) attached to the benzene ring.

Building block for organic synthesis

Used as a starting material in the preparation of various other organic compounds.

Used in pharmaceuticals and agrochemicals

It is used in the production of drugs and chemicals used in agriculture.

Precursor in the synthesis of dyes and pigments

It can be used as a starting material to make dyes and pigments.

Potentially hazardous

It is considered to be potentially dangerous, and proper safety precautions should be taken when handling and using it.

Check Digit Verification of cas no

The CAS Registry Mumber 17061-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,6 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17061-85:
(7*1)+(6*7)+(5*0)+(4*6)+(3*1)+(2*8)+(1*5)=97
97 % 10 = 7
So 17061-85-7 is a valid CAS Registry Number.

17061-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-nitro-4-prop-2-ynoxybenzene

1.2 Other means of identification

Product number -
Other names 4-(prop-2-ynyloxy)nitrobenzene

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:17061-85-7 SDS

17061-85-7Relevant articles and documents

Polymer nanocomposites using click chemistry: Novel materials for hydrogen peroxide vapor sensors

Mazumdar, Payal,Rattan, Sunita,Mukherjee, Monalisa

, p. 69573 - 69582 (2015)

Herein, we report the synthesis of nanocomposites (NCs) prepared by azide-functionalized polystyrene (Az-f-PS) coupled with alkyne-functionalized nanographite platelets (Alk-f-NGPs) by using copper(i) catalyzed azide-alkyne click chemistry. Linear polysty

PREPARATION, CRYSTAL STRUCTURE AND DIELECTRIC PROPERTIES OF THE NEW UNSYMMETRICALLY SUBSTITUTED DIACETYLENES NP/R2.

Strohriegl,Schultes,Heindl,Gruner-Bauer,Enkelmann,Dormann

, p. 918 - 924 (1987)

We report on the preparation, the crystal structure and the dielectric properties of several new unsymmetrically substituted diacetylenes R//1 minus C EQUVLNT C-C EQUVLNT C-R//2 of the general constitution NP/R//2. They carry a polar nitrophenoxy-group on

New phenoxymethyl substituted mesoionic triazolium salts: Synthesis and structural characterisation

Dhimba, George,Lawal, Nasir S.,Bala, Muhammad D.

, p. 100 - 107 (2019)

A new set of mesoionic 1,2,3-triazolium salts functionalised by para substituted phenoxymethyl side groups were prepared using the ‘click’ Cu catalyzed [3 + 2] cycloaddition of organic azides and terminal alkynes. Four previously unreported neutral triazoles (1–4) were first isolated en route to formation of the salts (5–8). All the compounds were fully characterised (1H, 13C NMR; IR; HR-MS; EA) and representative neutral triazoles and salts were structurally characterised by single crystal X-ray diffraction (SCXRD). Full examination of structural characteristics of the neutral compounds and the salts were presented by detailed analysis of multinuclear NMR data and SCXRD. As metal-free catalysts for the transfer hydrogenation of ketones to alcohols in isopropanol as solvent and hydrogen source, salts 5–8 showed moderate activities for the transformation of acetophenone to 1-phenyl alcohol.

Functionalization of single-walled carbon nanotubes with well-defined polystyrene by "click" coupling

Li, Huaming,Cheng, Fuyong,Duft, Andy M.,Adronov, Alex

, p. 14518 - 14524 (2005)

Covalent functionalization of alkyne-decorated SWNTs with well-defined, azide-terminated polystyrene polymers was accomplished by the Cu(I)-catalyzed [3 + 2] Huisgen cycloaddition. This reaction was found to be extremely efficient in producing organosolub

Four-component, one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles bearing 1-(2-phenylselenocyclohexyl) group

Sheng, Wusheng,Sheng, Shouri,Zeng, Jiangbo,Huang, Zhenzhong,Cai, Mingzhong

, p. E222-E226 (2014)

An efficient, one-pot, three-step, regioselective synthesis of 4-substituted 1-(2-phenylselenocyclohexyl)-1,2,3-triazoles, involving in situ generation of l-azido-2-phenylselenocyclohexane has been developed via four-component reaction of phenylselenenyl

Synthesis of sorafenib analogues incorporating a 1,2,3-triazole ring and cytotoxicity towards hepatocellular carcinoma cell lines

Palakhachane, Sarinya,Ketkaew, Yuwaporn,Chuaypen, Natthaya,Sirirak, Jitnapa,Boonsombat, Jutatip,Ruchirawat, Somsak,Tangkijvanich, Pisit,Suksamrarn, Apichart,Limpachayaporn, Panupun

supporting information, (2021/04/15)

A series of 1,2,3-triazole-containing Sorafenib analogues, in which the aryl urea moiety of Sorafenib (1) was replaced with a 1,2,3-triazole ring linking a substituted phenoxy fragment, were prepared successfully via Huisgen 1,3-dipolar cycloaddition and

Preparation method and application of propyne aryl ether compound

-

Paragraph 0073-0074, (2021/08/28)

The invention particularly relates to a method for preparing propyne aryl ether compounds from aryl phenol, halogenated propyne and derivatives of the halogenated propyne, and belongs to the technical field of preparation of the propyne aryl ether compoun

COMPOUNDS AND METHOD FOR TREATING CYTOKINE RELEASE SYNDROME

-

Page/Page column 108, (2021/02/12)

Disclosed herein are embodiments of a method for treating or preventing cytokine release syndrome (CRS). In certain embodiments, the method comprises administering a compound, or a salt, solvate, prodrug or pharmaceutical composition thereof, to a subject experiencing, or at risk of developing, CRS. The compound may be a kinase inhibitor, such as a JAK inhibitor and/or an IRAK inhibitor, and/or the compound may have a structure according to Formulas I, III, IV or VII. And the method may comprise administering the compound to a subject who is has received, is currently receiving, and/or will be receiving a cell therapy.

Azoacetylenes for the Synthesis of Arylazotriazole Photoswitches

Anderl, Felix,Balkenhohl, Moritz,Carreira, Erick M.,Fink, Moritz,Pfaff, Patrick

supporting information, p. 14495 - 14501 (2021/09/18)

We report a modular approach toward novel arylazotriazole photoswitches and their photophysical characterization. Addition of lithiated TIPS-acetylene to aryldiazonium tetrafluoroborate salts gives a wide range of azoacetylenes, constituting an underexplored class of stable intermediates.In situdesilylation transiently leads to terminal arylazoacetylenes that undergo copper-catalyzed cycloadditions (CuAAC) with a diverse collection of organoazides. These include complex molecules derived from natural products or drugs, such as colchicine, taxol, tamiflu, and arachidonic acid. The arylazotriazoles display near-quantitative photoisomerization and long thermalZ-half-lives. Using the method, we introduce for the first time the design and synthesis of a diacetylene platform. It permits implementation of consecutive and diversity-oriented approaches linking two different conjugants to independently addressable acetylenes within a common photoswitchable azotriazole. This is showcased in the synthesis of several photoswitchable conjugates, with potential applications as photoPROTACs and biotin conjugates.

Novel ferrocene-based 1,2,3-triazolyl compounds: Synthesis, anti-migration properties and catalytic effects on oxidizers during combustion

Cheng, Wenqian,Shi, Xiaoling,Zhang, Yu,Jian, Yajun,Zhang, Guofang

, (2019/12/26)

To tackle high-migratory and high-volatility problem of marketed neutral ferrocene-based burning rate catalysts, twenty-one ferrocene-based 1,2,3-triazolyl compounds (Fc-TAZs) were synthesized by click reaction and characterized completely by NMR, FT-IR,

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 17061-85-7