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

39501-62-7

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39501-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39501-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,0 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 39501-62:
(7*3)+(6*9)+(5*5)+(4*0)+(3*1)+(2*6)+(1*2)=117
117 % 10 = 7
So 39501-62-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO2/c14-13-10-6-8-12(9-7-10)15-11-4-2-1-3-5-11/h1-9,13-14H

39501-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-phenoxyphenyl)hydroxylamine

1.2 Other means of identification

Product number -
Other names N-(p-Phenoxyphenyl)hydroxylamine

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:39501-62-7 SDS

39501-62-7Upstream product

39501-62-7Relevant academic research and scientific papers

Expeditious and Efficient ortho-Selective Trifluoromethane-sulfonylation of Arylhydroxylamines

Liu, Yue,Bai, Songlin,Du, Yuanbo,Qi, Xiangbing,Gao, Hongyin

supporting information, (2021/12/27)

A metal- and oxidant-free, practical and efficient method for the synthesis of highly versatile and synthetically useful ortho-trifluoromethanesulfonylated anilines from arylhydroxylamines and trifluoromethanesulfinic chloride was developed. This rapid tr

Cascade Approach to Highly Functionalized Biaryls by a Nucleophilic Aromatic Substitution with Arylhydroxylamines

Guo, Lirong,Liu, Fengting,Wang, Liying,Yuan, Hairui,Feng, Lei,Kürti, László,Gao, Hongyin

supporting information, p. 2894 - 2898 (2019/04/25)

A transition-metal free synthesis of highly functionalized 2-hydroxy-2′-amino-1,1′-biaryls from N-arylhydroxylamines has been developed. This operationally simple and readily scalable approach relies on a cascade of reactions that initially generates transient N,O-diarylhydroxylamines, via direct O-arylation, which then undergo rapid [3,3]-sigmatropic rearrangement and subsequent rearomatization to form NOBIN-type products. These structurally diverse functionalized biaryls are obtained under mild conditions in good to excellent isolated yields.

Glycosides of N-Hydroxy-N-arylamine Derivatives. Part 2. Convenient Synthetic Methods for N-Glycosides of N-Hydroxy-N-arylamines

Yoshioka, Tadao,Yamada, Hidetoshi,Uematsu, Takayoshi

, p. 1271 - 1276 (2007/10/02)

Two convenient methods for the synthesis of N-glucuronides of N-hydroxy-N-arylamines, (8a-e) and (9a), have been developed.N-Hydroxy-N-arylamines (6a-e) were condensed with triethylammonium D-glucopyranuronate (4) to give 1-deoxy-1-(N-hydroxy-N-arylamino)

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