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2-[1-(phenylamino)ethyl]phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60399-07-7

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60399-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60399-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,9 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60399-07:
(7*6)+(6*0)+(5*3)+(4*9)+(3*9)+(2*0)+(1*7)=127
127 % 10 = 7
So 60399-07-7 is a valid CAS Registry Number.

60399-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-anilinoethyl)phenol

1.2 Other means of identification

Product number -
Other names 2,6-DIBROMO-9,9,10,10-TETRAMETHYL-9,10-DIHYDRO-ANTHRACENE

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:60399-07-7 SDS

60399-07-7Relevant academic research and scientific papers

Synthesis and Anti-Fungal Activity of New 3-Aryl-1,3-benzoxazine-2-ketone Derivatives

Huang, Fen,Jiao, Wenjie,Wan, Yichao

, p. 1112 - 1116 (2021/08/06)

Abstract: In the study, a series of new 3-aryl-1,3-benzoxazine-2-ketone derivatives hasbeen designed, synthesized and evaluated for anti-fungal activity against sixspecies of phytopathogenic fungi. Among those, two compounds have exhibited highinhibitory

Oxazine Ring-Related Vibrational Modes of Benzoxazine Monomers Using Fully Aromatically Substituted, Deuterated, 15N Isotope Exchanged, and Oxazine-Ring-Substituted Compounds and Theoretical Calculations

Han, Lu,Iguchi, Daniela,Gil, Phwey,Heyl, Tyler R.,Sedwick, Victoria M.,Arza, Carlos R.,Ohashi, Seishi,Lacks, Daniel J.,Ishida, Hatsuo

, p. 6269 - 6282 (2017/09/01)

Polymerization of benzoxazine resins is indicated by the disappearance of a 960-900 cm-1 band in infrared spectroscopy (IR). Historically, this band was assigned to the C-H out-of-plane bending of the benzene to which the oxazine ring is attach

EPR and ENDOR Study of Chiral Nitroxides

Stegmann, Hartmut B.,Schaber, Frank-Martin,Schuler, Paul,Scheffler, Klaus

, p. 887 - 891 (2007/10/02)

Racemic and achiral alkyl aryl nitroxides were examined at various temperatures.The restricted rotation of the aminoxyl substituents was indicated both by the β-proton coupling constants and by the inequivalence of the aromatic ortho protons.These results

New Route for the Preparation of 2H-3-Aryl-3,4-dihydro-1,3-benzoxazines and 2H-3-Aryl-3,4-dihydro-4-methyl-1,3-benzoxazines

Joglekar, S. J.,Samant, S. D.

, p. 110 - 111 (2007/10/02)

2-Hydroxybenzaldehyde (1) and 1-(2-hydroxyphenyl)ethanone (2) on reaction with different primary aromatic amines gave 2-(arylimino)methylphenols (3) and 2-phenols (4), respectively. 3 and 4 on reduction with sodium borohydride gave 2-(arylamino)methylphenols (5) and 2-phenols (6), which underwent cyclisation with formaldehyde to form 2H-3-aryl-3,4-dihydro-1,3-benzoxazines (7) and 2H-3-aryl-3,4-dihydro-4-methyl-1,3-benzoxazines (8), respectively.

Syntheses d'aminoalcools-1,3 ou d'aminophenols-1,3 par reduction d'enaminones ou d'iminophenols par les hydrures metalliques. Etude structurale par infrarouge et RMN des aminoalcools-1,3 bisecondaires diastereomeres

Maroni, Pierre,Cazaux, Louis,Tisnes, Pierre,Zambeti,Marianthie

, p. 179 - 186 (2007/10/02)

Enaminones, obtained by reaction of a primary amine with a β-diketone, can take three tautomeric forms: keto-enamine Ia, keto-imine Ib and imino-enol Ic.In general the keto-enamine form Ia is the most stable.Thi

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