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4-tert-butyl-N-(3-methoxyphenyl)benzamide is a chemical compound with the molecular formula C18H21NO3. It is a derivative of benzamide, featuring a tert-butyl group at the 4-position and a 3-methoxyphenyl group attached to the nitrogen atom. 4-tert-butyl-N-(3-methoxyphenyl)benzamide is known for its potential applications in pharmaceutical research, particularly as a precursor or intermediate in the synthesis of various bioactive molecules. Its structure provides a balance of lipophilicity and polarity, which can be crucial for drug design. The compound's properties, such as solubility and stability, can be influenced by the presence of the tert-butyl and methoxy groups, making it a versatile building block in the development of new therapeutic agents.

5331-94-2

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5331-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5331-94-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5331-94:
(6*5)+(5*3)+(4*3)+(3*1)+(2*9)+(1*4)=82
82 % 10 = 2
So 5331-94-2 is a valid CAS Registry Number.

5331-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-tert-butyl-N-(3-methoxyphenyl)benzamide

1.2 Other means of identification

Product number -
Other names Anthranilsaeure,Kupfersalz

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:5331-94-2 SDS

5331-94-2Relevant academic research and scientific papers

Thermal investigation of the compounds of the copper(II) mono(o-hydroxybenzoate) with chelate ligands

Olczak-Kobza

, p. 989 - 993 (2008/10/08)

Heteroligand complexes of copper(II) were obtained as a result of the reaction of Cu(II) mono (o-hydroxybenzoate) (monohydrate) with 8-hydroxyquinoline (HOx), o-aminophenol (NH2Ph) and 2,2'-dipyridyl (2,2'-dipy). The mixture of the mono compound with: Cu(II) di(o-aminobenzoate) or Cu(II) di(o-hydroxybenzaldoximate) were obtained by the reaction with o-aminobenzoic acid (H2A) and o-hydroxybenzaldoxime (H2Salox). The obtained compounds and their sinters were subjected to chemical, X-ray and thermal analyses.

SOLID STATE REACTIVITY OF ORGANIC COMPOUNDS WITH INORGANIC COMPOUNDS I. REACTIONS OF CUPRIC ACETATE AND COPPER CARBONATE WITH 2-, 3-, AND 4-AMINOBENZOIC ACIDS.

Bassi,Chopra

, p. 253 - 260 (2008/10/08)

The reactions of 2-, 3-, and 4-aminobenzoic acids with copper acetate and basic copper carbonate were studied in the solid state. The products have been identified as bis(aminobenzoato) copper(II) complexes. Kinetic data for the reactions have been record

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