889676-36-2

Basic information

• Product Name: N,N-DIETHYL 4-BROMO-3-METHOXYBENZAMIDE 98
• Synonyms: N,N-DIETHYL 4-BROMO-3-METHOXYBENZAMIDE 98;N,N-Diethyl-4-bromo-3-methoxybenzamide 98%
• CAS NO: 889676-36-2
• Molecular Formula: C₁₂H₁₆BrNO₂
• Molecular Weight: 286.1674
• Product Categories: blocks;Bromides;Carboxes
• Mol File: 889676-36-2.mol
• Article Data: 1

Chemical Properties

• Melting Point: 68-70
• Boiling Point: 392.3 °C at 760 mmHg
• Flash Point: 191.1 °C
• Appearance: /
• Density: 1.313 g/cm³
• Vapor Pressure: 2.31E-06mmHg at 25°C
• Refractive Index: 1.539
• Storage Temp.: Keep Cold
• CAS DataBase Reference: N,N-DIETHYL 4-BROMO-3-METHOXYBENZAMIDE 98(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-DIETHYL 4-BROMO-3-METHOXYBENZAMIDE 98(889676-36-2)
• EPA Substance Registry System: N,N-DIETHYL 4-BROMO-3-METHOXYBENZAMIDE 98(889676-36-2)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 889676-36-2(Hazardous Substances Data)

Usage

General Description

N,N-Diethyl 4-bromo-3-methoxybenzamide 98 is a chemical compound used in various industrial and research applications. It is a derivative of benzamide that contains a 4-bromo-3-methoxy group and a diethyl amine moiety. N,N-DIETHYL 4-BROMO-3-METHOXYBENZAMIDE 98 is commonly used as a building block for the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is known for its high purity level of 98% and is a popular choice for laboratories and research facilities. It should be handled and stored in accordance with proper safety protocols and regulations.

InChI:InChI=1/C12H16BrNO2/c1-4-14(5-2)12(15)9-6-7-10(13)11(8-9)16-3/h6-8H,4-5H2,1-3H3

Upstream product

• 56256-14-5 4-bromo-3-methoxy-benzoic acid 
• 530-62-1 1,1'-carbonyldiimidazole 

Downstream Products

• 1403330-33-5 N,N-diethyl-4-{[6-(4-{[(4-fluorophenyl)acetyl]amino}phenyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino}-3-methoxybenzamide 

Relevant articles and documents

Synthesis of18F-Difluoromethylarenes from Aryl (Pseudo) Halides

A general method for the synthesis of [18F]difluoromethylarenes from [18F]fluoride for radiopharmaceutical discovery is reported. The method is practical, operationally simple, tolerates a wide scope of functional groups, and enables the labeling of a variety of arenes and heteroarenes with radiochemical yields (RCYs, not decay-corrected) from 10 to 60 %. The18F-fluorination precursors are readily prepared from aryl chlorides, bromides, iodides, and triflates. Seven18F-difluoromethylarene drug analogues and radiopharmaceuticals including Claritin, fluoxetine (Prozac), and [18F]DAA1106 were synthesized to show the potential of the method for applications in PET radiopharmaceutical design.