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52671-42-8

4-nitrosodiphenyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52671-42-8 Structure

  • Basic information

    1. Product Name: 4-nitrosodiphenyl ether
    2. Synonyms: 4-nitrosodiphenyl ether
    3. CAS NO:52671-42-8
    4. Molecular Formula: C12H9NO2
    5. Molecular Weight: 199.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52671-42-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 313.1°Cat760mmHg
    3. Flash Point: 146.1°C
    4. Appearance: /
    5. Density: 1.12g/cm3
    6. Vapor Pressure: 0.000935mmHg at 25°C
    7. Refractive Index: 1.568
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-nitrosodiphenyl ether(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-nitrosodiphenyl ether(52671-42-8)
    12. EPA Substance Registry System: 4-nitrosodiphenyl ether(52671-42-8)

  • 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: 52671-42-8(Hazardous Substances Data)

52671-42-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52671-42-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,7 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52671-42:
(7*5)+(6*2)+(5*6)+(4*7)+(3*1)+(2*4)+(1*2)=118
118 % 10 = 8
So 52671-42-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO2/c14-13-10-6-8-12(9-7-10)15-11-4-2-1-3-5-11/h1-9H

52671-42-8SDS

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 1-Nitroso-4-phenoxybenzene

1.2 Other means of identification

Product number -
Other names -

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:52671-42-8 SDS

52671-42-8Relevant articles and documents

Ipso-Nitrosation of arylboronic acids with chlorotrimethylsilane and sodium nitrite

Prakash, G.K. Surya,Gurung, Laxman,Schmid, Philipp Christoph,Wang, Fang,Thomas, Tisa Elizabeth,Panja, Chiradeep,Mathew, Thomas,Olah, George A.

, p. 1975 - 1978 (2014/04/03)

Nitroso compounds are versatile reagents in synthetic organic chemistry. Herein, we disclose a feasible protocol for the ipso-nitrosation of aryl boronic acids using chlorotrimethylsilane-sodium nitrite unison as nitrosation reagent system.

A highly stereoselective organocatalytic tandem aminoxylation/aza-Michael reaction for the synthesis of tetrahydro-1,2-oxazines

Zhu, Di,Lu, Min,Chua, Pei Juan,Tan, Bin,Wang, Fei,Yang, Xinhao,Zhong, Guofu

supporting information; experimental part, p. 4585 - 4588 (2009/05/13)

(Chemical Equation Presented) A facile stereoselective synthesis of multifunctionalized tetrahydro-1,2-oxazines (THOs) has been achieved by the organocatalyzed asymmetric tandem α-aminoxylation/aza-Michael reaction for the C-O/C -N bond formations in moderate to good yields with excellent diastereo- (>99:1 dr) and enantioselectivities (92% to >99% ee).

Diastereo- and enantioselective synthesis of nitroso Diels-Alder-type bicycloketones using dienamine: Mechanistic insight into sequential nitroso aldol/Michael reaction and application for optically pure 1-amino-3,4-diol synthesis

Momiyama, Norie,Yamamoto, Yuhei,Yamamoto, Hisashi

, p. 1190 - 1195 (2007/10/03)

This article presents complete diastereo- and highly enantioselective synthesis of nitroso Diels-Alder-type bicycloketones using dienamine. With the hydrogen bonding of two hydroxyls in the bulky binaphthol 1c, high enantioselectivities and complete diast

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