35306-75-3

Basic information

• Product Name: 3-Bromo-N-isopropylbenzamide
• Synonyms: 3-Bromo-N-isopropylbenzamide;3-bromo-N-isopropylbenzamide(SALTDATA: FREE)
• CAS NO: 35306-75-3
• Molecular Formula: C₁₀H₁₂BrNO
• Molecular Weight: 242.11
• Product Categories: blocks;Bromides;Carboxes
• Mol File: 35306-75-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 335.1°Cat760mmHg
• Flash Point: 156.4°C
• Appearance: /
• Density: 1.349g/cm³
• Vapor Pressure: 0.000123mmHg at 25°C
• Refractive Index: 1.545
• CAS DataBase Reference: 3-Bromo-N-isopropylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Bromo-N-isopropylbenzamide(35306-75-3)
• EPA Substance Registry System: 3-Bromo-N-isopropylbenzamide(35306-75-3)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 35306-75-3(Hazardous Substances Data)

Usage

General Description

3-Bromo-N-isopropylbenzamide is a chemical compound with the molecular formula C10H12BrNO. It is a white to off-white crystalline solid that is commonly used as an intermediate in the synthesis of pharmaceuticals. 3-Bromo-N-isopropylbenzamide is known for its use in the preparation of various drugs such as NSAIDs (nonsteroidal anti-inflammatory drugs) and anticancer agents. It is also utilized in the field of organic chemistry for the synthesis of diverse heterocyclic compounds. 3-Bromo-N-isopropylbenzamide has been studied for its potential therapeutic applications and shows promise for its use in the development of new pharmaceuticals. Its unique chemical properties make it a valuable building block for the synthesis of various biologically active compounds.

InChI:InChI=1/C10H12BrNO/c1-7(2)12-10(13)8-4-3-5-9(11)6-8/h3-7H,1-2H3,(H,12,13)

Upstream product

• 1711-09-7 3-bromobenzoyl chloride 
• 75-31-0 isopropylamine 
• 35309-72-9 N,N-diisopropyl-3-bromobenzamide 

Downstream Products

• 65262-68-2 3-(4-Chloro-3,5-dimethyl-phenoxy)-N-isopropyl-benzamide 
• 65262-24-0 N-Isopropyl-3-(2-chlorophenoxy)-benzamid 
• 65262-77-3 N-Isopropyl-3-(3-chloro-5-methoxyphenoxy)-benzamid 
• 2415-93-2 1-(3-bromophenyl)-2-methylpropane-1-one 
• 898769-06-7 (3-bromophenyl)(cyclohexyl)methanone 
• 6952-59-6 3-cyanobromobenzene 
• 65262-59-1 3-(4-Chloro-2-methyl-phenoxy)-N-isopropyl-benzamide 
• 65261-74-7 3-(2-sec-Butyl-phenoxy)-N-isopropyl-benzamide 

Relevant articles and documents

Chemoselective Synthesis of α-Amino-α-cyanophosphonates by Reductive Gem-Cyanation-Phosphonylation of Secondary Amides

A novel approach to α-amino-α-cyanophosphonates has been developed. The method features a Tf2O-mediated reductive geminal cyanation/phosphonylation of secondary amides. Mild reaction conditions, high bond-forming efficiency, inexpensive readily available starting materials, and good to excellent yields with wide functional group compatibility constitute the main advantages of this method. The protocol can be run on a gram scale.

1-substituted phenyl-1-(1h-imidazol-4-yl) alcohols, process for producing the same and use thereof

To provide a composition having a steroid C17,20-lyase inhibitory activity and useful as an agent for the prophylaxis or treatment of prostatism and tumors such as breast cancer. A compound represented by the formula: wherein R is a hydrogen atom or a protecting group, R1is a lower alkyl group or a cyclic hydrocarbon group, R2is an aromatic hydrocarbon group optionally having substituents or an aromatic heterocyclic group optionally having substituents, R3is a hydrocarbon group optionally having substituents, a hydroxyl group optionally having substituents, a thiol group optionally having substituents, an amino group optionally having substituents, an acyl group or a halogen atom, and n is an integer of 0 to 4, and a salt thereof have a steroid C17,20-lyase inhibitory activity, and are useful as an agent for the pophylaxis or treatment of prostatism and tumors such as beast cancer and the like.