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Acetamide, 2-methoxy-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126191-21-7

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126191-21-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126191-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,1,9 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 126191-21:
(8*1)+(7*2)+(6*6)+(5*1)+(4*9)+(3*1)+(2*2)+(1*1)=107
107 % 10 = 7
So 126191-21-7 is a valid CAS Registry Number.

126191-21-7SDS

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 methoxy-acetic acid anilide

1.2 Other means of identification

Product number -
Other names Methoxy-essigsaeure-anilid

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:126191-21-7 SDS

126191-21-7Relevant academic research and scientific papers

Synthesis, physico-chemical properties and microsomal stability of compounds bearing aliphatic trifluoromethoxy group

Grygorenko, Oleksandr O.,Haufe, Günter,Kliachyna, Maria,Kondratov, Ivan S.,Logvinenko, Ivan G.,Markushyna, Yevheniia,Pivnytska, Valentyna,Tokaryeva, Yuliya,Vashchenko, Bohdan V.

, (2020/02/11)

Effects of the trifluoromethoxy substituent on physico-chemical properties of compounds, such as kinetic solubility, lipophilicity and microsomal clearance, was studied in a series of aliphatic derivatives. It was found that kinetic solubility of the CF3O-containing compounds was comparable to that of analogs, i.e. compounds bearing CH3O and CF3 moieties. The CF3O-substituted compounds had higher lipophilicity as compared to methoxy analogues, and nearly the same like CF3-bearing compounds. Microsomal stability studies indicated that the trifluoromethoxy group typically decreased metabolic stability of the corresponding derivatives as compared to either CH3O- or CF3-substituted counterparts, except for N-alkoxy(sulfon)amide series.

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