65136-50-7

Basic information

• Product Name: Benzoyl chloride, 4-(2-chloroethoxy)-
• CAS NO: 65136-50-7
• Molecular Formula: C9H8Cl2O2
• Molecular Weight: 219.067
• Mol File: 65136-50-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzoyl chloride, 4-(2-chloroethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 4-(2-chloroethoxy)-(65136-50-7)
• EPA Substance Registry System: Benzoyl chloride, 4-(2-chloroethoxy)-(65136-50-7)

Safety Data

• Hazardous Substances Data: 65136-50-7(Hazardous Substances Data)

Upstream product

• 120-47-8 Ethyl 4-hydroxybenzoate 
• 40992-21-0 4-(2-chloro-ethoxy)-benzoic acid ethyl ester 
• 38567-00-9 4-(2-Chloroethoxy)benzoic acid methyl ester 
• 79-37-8 oxalyl dichloride 
• 65136-51-8 4-(2-chloroethoxy)benzoic acid 
• 99-76-3 methyl 4-hydroxylbenzoate 
• 3204-73-7 4-(2-hydroxyethoxy)benzoic acid methyl ester 
• 10026-13-8 phosphorus pentachloride 
• 1711-24-6 4-(2-hydroxyethoxy)benzoic acid 

Downstream Products

• 65136-51-8 4-(2-chloroethoxy)benzoic acid 
• 1428437-92-6 (2-{4-[7-(benzyl-N-methylamino)heptyloxy]phenyl}benzofuran-3-yl)-[4-(2-chloroethoxy)phenyl]methanone 
• 1622204-11-8 5-((2-(4-(2-(4-hydroxypiperidin-1-yl)ethoxy)benzamide)pyridin-4-yl)oxy)-6-methoxy-N-methyl-1H-indole-1-carboxamide 
• 1622206-03-4 C₂₅H₂₃ClN₄O₅ 
• 84449-90-1 Raloxifen 
• 84541-38-8 [6-Methoxy-2-(4-Methoxyphenyl)benzo[b]thien-3-yl]-[4-[2-(1-Piperidinyl)ethoxy]phenyl] Methanone 
• 1449689-98-8 4-[4-(2-chloro-ethoxy)-phenyl]-7-methoxy-3-phenyl-1,2-dihydro-naphthalene 

Relevant articles and documents

Discovery of novel benzofuran-based compounds with neuroprotective and immunomodulatory properties for Alzheimer's disease treatment

To address the multifactorial nature of Alzheimer's Disease (AD), a multi-target-directed ligand approach was herein developed. As a follow-up of our previous studies, a small library of newly designed 2-arylbenzofuran derivatives was evaluated towards ch

Piperidine nucleophilic substitution without solvent: An efficient synthesis of raloxifene

Mild and high-yielding synthesis is described for raloxifene via piperdine nucleophilic substitution of a new raloxifene intermediate 3-aroyl-2-aryl-substituted benzo[b]thiophenes, which is obtained by acylation of para-substituted benzoyl chlorides and 2-arylbenzo[b]thiophenes. The key step is solvent free and offers valuable advantages, such as low cost, and is suitable for industrial production.

Benzothiophenes and related compounds as estrogen agonists

The invention is a compound of Formula (I): wherein R is —OH, R1is —OH, R2is —H, n is 2 or 3 and X is sulfur, or a pharmaceutically acceptable salt of a compound having Formula (1), or a pharmaceutical composition comprising a compou