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Benzamide, N-butyl-2-(4-morpholinylcarbonyl)is a chemical compound with a molecular formula C18H26N2O3. It is a morpholine derivative featuring a benzamide and N-butyl-substituted group. Benzamide, N-butyl-2-(4-morpholinylcarbonyl)is recognized for its diverse industrial and research applications, such as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also valued for its potent inhibitory effects on certain enzymes and receptors, making it a significant tool in biochemical research. Furthermore, it contributes to the field of medicinal chemistry through the development of new therapeutic agents, showcasing its versatility and importance in the scientific community.

104958-67-0

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104958-67-0 Usage

Uses

Used in Pharmaceutical Industry:
Benzamide, N-butyl-2-(4-morpholinylcarbonyl)is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its chemical structure allows for the creation of compounds with potential medicinal properties, making it an essential component in drug discovery and design.
Used in Agrochemical Industry:
In the agrochemical sector, Benzamide, N-butyl-2-(4-morpholinylcarbonyl)is employed as a precursor in the synthesis of agrochemicals. Its role in creating compounds with pesticidal or herbicidal properties aids in the development of more effective and targeted crop protection solutions.
Used in Biochemical Research:
Benzamide, N-butyl-2-(4-morpholinylcarbonyl)is used as a potent inhibitor of certain enzymes and receptors. This application makes it a valuable tool in biochemical research, where understanding the interactions between compounds and biological targets is crucial for advancing scientific knowledge and developing new therapeutic strategies.
Used in Medicinal Chemistry:
Benzamide, N-butyl-2-(4-morpholinylcarbonyl)is utilized in the field of medicinal chemistry for the development of new therapeutic agents. Its unique properties and functions enable the creation of novel compounds with potential applications in treating various diseases and medical conditions, highlighting its importance in the ongoing pursuit of innovative healthcare solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 104958-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,5 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104958-67:
(8*1)+(7*0)+(6*4)+(5*9)+(4*5)+(3*8)+(2*6)+(1*7)=140
140 % 10 = 0
So 104958-67-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H22N2O3/c1-2-3-8-17-15(19)13-6-4-5-7-14(13)16(20)18-9-11-21-12-10-18/h4-7H,2-3,8-12H2,1H3,(H,17,19)

104958-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-butyl-2-(morpholine-4-carbonyl)benzamide

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:104958-67-0 SDS

104958-67-0Downstream Products

104958-67-0Relevant academic research and scientific papers

REACTION OF N-SUBSTITUTED PHTHALIMIDES AND ISOPHTHALIMIDES WITH SECONDARY AMINES

Ganin, E. V.,Makarov, V. F.,Rozynov, B. V.

, p. 2205 - 2208 (2007/10/02)

The N,N'-substituted diamides of phthalic acid are formed in the reaction of N-substituted phthalimides and isophthalimides with secondary amines.The isophthalimides are stronger agents.Cyclic amines with a medium ring size are acylated so readily that the reaction of 2-bromoethylphthalimide with piperidine leads primarily to the acylation product.

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