34249-94-0

Basic information

• Product Name: Benzamide, 2-(oxiranylmethoxy)-
• CAS NO: 34249-94-0
• Molecular Formula: C10H11NO3
• Molecular Weight: 193.202
• Mol File: 34249-94-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzamide, 2-(oxiranylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 2-(oxiranylmethoxy)-(34249-94-0)
• EPA Substance Registry System: Benzamide, 2-(oxiranylmethoxy)-(34249-94-0)

Safety Data

• Hazardous Substances Data: 34249-94-0(Hazardous Substances Data)

Upstream product

• 65-45-2 salicylamide 
• 106-89-8 epichlorohydrin 
• 58027-55-7 3-chloro-1-(2-carbamoylphenoxy)propan-2-ol 

Downstream Products

• 131620-19-4 2-(2-hydroxy-3-succinimido-propoxy)-benzoic acid amide 
• 101732-20-1 2-(2-hydroxy-3-phthalimido-propoxy)-benzoic acid amide 
• 66817-05-8 2-{2-Hydroxy-3-[2-(2-phenylacetylamino-acetylamino)-ethylamino]-propoxy}-benzamide 
• 58714-61-7 1-(2-Propylamino)-3-(2-carboxamidophenoxy)propan-2-ol 
• 58827-35-3 Thiophene-2-carboxylic acid {2-[3-(2-carbamoyl-phenoxy)-2-hydroxy-propylamino]-ethyl}-amide 
• 72742-63-3 2-[2-hydroxy-3-[[2-(3-indolyl)-1,1-dimethylethyl]amino]propoxy]benzamide 
• 50448-56-1 C₂₆H₃₈N₄O₆ 
• 66825-00-1 2-[3-(2-Amino-ethylamino)-2-hydroxy-propoxy]-benzamide 
• 58027-38-6 1-o-carbamoylphenoxy-3-β-(3-phenylureido)ethylamino-2-propanol 
• 58027-41-1 2-{3-[2-(3-Allyl-ureido)-ethylamino]-2-hydroxy-propoxy}-benzamide 
• 58027-42-2 2-{2-Hydroxy-3-[2-(propane-1-sulfonylamino)-ethylamino]-propoxy}-benzamide 
• 58027-40-0 2-[2-Hydroxy-3-(2-phenylacetylamino-ethylamino)-propoxy]-benzamide 
• 58027-57-9 2-[3-(6-Hexanoylamino-hexylamino)-2-hydroxy-propoxy]-benzamide 
• 58027-39-7 3-<(2-isobutyramidoethyl)amino>-1-(2-carbamoylphenoxy)propan-2-ol 

Relevant articles and documents

Antihypertensive indole derivatives of phenoxypropanolamines with β-adrenergic receptor antagonist and vasodilating activity

A series of 25 aryloxypropanolamines containing the 3-indolyl-tert-butyl[i.e., 1,1-dimethyl-2-(1H-indol-3-yl)ethyl] or substituted 3-indolyl-tert-butyl moiety as the N substituent is reported. These compounds have been tested for antihypertensive activity in spontaneously hypertensive rats (SHR), β-adrenergic receptor antagonist action in conscious normotensive rats, vasodilating activity in ganglion-blocked rats with blood pressure maintained by angiotensin II infusion, and for intrinsic sympathomimetic action (ISA) in reserpinized rats. Some of the compounds exhibit antihypertensive activity in combination with β-adrenergic receptor antagonist and vasodilating action. The structure-activity relationships in these tests are discussed.