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Phenol, 4-nitro-, compd. with N,N-diethylethanamine (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15852-96-7

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15852-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15852-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,5 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15852-96:
(7*1)+(6*5)+(5*8)+(4*5)+(3*2)+(2*9)+(1*6)=127
127 % 10 = 7
So 15852-96-7 is a valid CAS Registry Number.

15852-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name p-nitrophenol-triethylamine complex (hydrogen-bonded complex)

1.2 Other means of identification

Product number -
Other names p-nitrophenol-triethylamine complex (proton-transfer complex)

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:15852-96-7 SDS

15852-96-7Relevant academic research and scientific papers

Photo-/Baso-Chromisms and the Application of a Dual-Addressable Molecular Switch

Liu, Danyang,Yu, Binhong,Su, Xing,Wang, Xiaojun,Zhang, Yu-Mo,Li, Minjie,Zhang, Sean Xiao-An

supporting information, p. 2838 - 2845 (2019/07/18)

Two typical molecular switches of spiropyran (SP) and benzoxazine (OX) were fused by sharing an indole to achieve a new dual-addressable molecular switch (SP-OX-NO2). Through proper molecular modification with NO2, the transformation

Determination of basic strength of aliphatic amines through ion pair formation in some ionic liquid solutions

D'Anna, Francesca,Vitale, Paola,Noto, Renato

experimental part, p. 6224 - 6230 (2009/12/08)

(Chemical Equation Presented) To have an evaluation of the basic strength of aliphatic amines in ionic liquid solution, the stability constants relevant to the formation of amine/p-nitrophenol ion pairs were determined in different ionic liquids at 298 K.

Proton-Transfer Equilibria between Notrophenols and Alkylamines in N-Methylformamide

Oncescu, T.,Oancea, A.-M.,Maeyer, L. De

, p. 2593 - 2599 (2007/10/02)

The equilibrium constants, Ke, of the proton-transfer reactions between o-, m-, and p-nitrophenols (ONP, MNP, and PNP, respectively), and monomethylamine and di- and triethylamines (MNA, DEA, and TEA, respectively) in N-methylformamide (NMF) were measured spectrophotometrically by using amine-amine hydrochloride buffers at different temperatures and 0.1-0.2 M ionic strength.Together with the previously measured pKa of p-nitrophenol, these values allowed the determination of the acidity constants of alkylamines and the other nitrophenols in this solvent.The reported values are compared with literature data in other media including the gas phase.The reaction enthalpies and entropies are also reported and discussed for some of these systems.

Rates of Reaction in the p-Nitrophemol-Triethylamine System in Acetonitrile

Marshall, David B.,Strohbusch, Frank,Eyring, Edward M.

, p. 2270 - 2273 (2007/10/02)

The rate constants of proton transfer between p-nitrophenol (AH) and triethylamine (B) in acetonitrile (ionic strength μ1.3E-4 M, 25.0 deg C) were measured by the electric field jump relaxation method with spectrophotometric detection.This acid-base syst

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