74993-52-5

Basic information

• Product Name: Hydroxylamine, O-(3-methylphenyl)-
• CAS NO: 74993-52-5
• Molecular Formula: C7H9NO
• Molecular Weight: 123.155
• Mol File: 74993-52-5.mol
• Article Data: 21

Chemical Properties

• Boiling Point: 65 °C(Press: 5 Torr)
• Density: 1.053±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Hydroxylamine, O-(3-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Hydroxylamine, O-(3-methylphenyl)-(74993-52-5)
• EPA Substance Registry System: Hydroxylamine, O-(3-methylphenyl)-(74993-52-5)

Safety Data

• Hazardous Substances Data: 74993-52-5(Hazardous Substances Data)

Upstream product

• 1239023-69-8 C₂₆H₁₅F₁₇N₂O₄ 
• 17933-03-8 m-tolylboronic acid 
• 937716-84-2 N-(3-methyl)phenoxyphthalimide 
• 108-39-4 3-methyl-phenol 

Downstream Products

• 95-71-6 2-methylbenzene-1,4-diol 
• 39267-61-3 2,2,2-trifluoro-N-(2-hydroxy-4-methylphenyl)acetamide 
• 452-86-8 4-methyl-1,2-dihydroxybenzene 
• 937716-65-9 (E)-1-phenylethanone O-(3-methylphenyl)oxime 
• 14770-90-2 2,3-diphenyl-6-methylbenzofuran 
• 1443440-55-8 N-(m-tolyloxy)acetamide 
• 39720-17-7 2-(2'-hydroxy-4'-methylphenyl)benzoxazole 
• 3098-18-8 2-hydroxy-4-methylbenzophenone 
• 13429-10-2 N-(2-hydroxy-4-methylphenyl)acetamide 
• 65109-84-4 1-benzoyl-4-methylcatechol 
• 74993-56-9 N-m-Tolyloxy-benzamide 
• 2835-97-4 2-amino-3-methylphenol 

Relevant articles and documents

An Activity-Based Sensing Fluorogenic Probe for Monitoring Ethylene in Living Cells and Plants

Ethylene (ET) is an important gaseous plant hormone. It is highly desirable to develop fluorescent probes for monitoring ethylene in living cells. We report an efficient RhIII-catalysed coupling of N-phenoxyacetamides to ethylene in the presenc

Rhodium(III)-Catalyzed Enantio- and Diastereoselective C?H Cyclopropylation of N-Phenoxylsulfonamides: Combined Experimental and Computational Studies

Cyclopropane rings are a prominent structural motif in biologically active molecules. Enantio- and diastereoselective construction of cyclopropanes through C?H activation of arenes and coupling with readily available cyclopropenes is highly appealing but

RhIII-Catalyzed Decarboxylative o-Acylation of Arenes Bearing an Oxidizing Directing Group

Here in we report, rhodium(III)-catalyzed decarboxylative acylation of arenes using α-oxocarboxylic acids as acyl surrogate. In this strategy, O–NHAc group act as an autocleavable oxidizing directing group (ODGauto), thus giving rise to ortho-acylated phenols in moderate to good yields. Mechanistic studies provided strong support for a kinetically relevant C–H bond activation. According to the best of our knowledge, this is the first report of Rhodium catalyzed decarboxylative acylation.