162155-27-3

Basic information

• Product Name: 3-amino-5-methoxyphenol
• Synonyms: 3-amino-5-methoxyphenol
• CAS NO: 162155-27-3
• Molecular Formula: C₇H₉NO₂
• Molecular Weight: 139.15186
• Mol File: 162155-27-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 332.0±22.0 °C(Predicted)
• Appearance: /
• Density: 1.219±0.06 g/cm3(Predicted)
• Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
• PKA: 9?+-.0.10(Predicted)
• CAS DataBase Reference: 3-amino-5-methoxyphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-amino-5-methoxyphenol(162155-27-3)
• EPA Substance Registry System: 3-amino-5-methoxyphenol(162155-27-3)

Safety Data

• Hazardous Substances Data: 162155-27-3(Hazardous Substances Data)

Upstream product

• 10272-07-8 3.5-dimethoxyaniline 

Downstream Products

• 1161837-78-0 N-acetyl-S-[4-(3-hydroxy-5-methoxyphenyl-1-yl)-aminoquinolin-6-yl]-S-methylsulphoximide 
• 1161837-82-6 N-(ethylamino)carbonyl-S-[4-(3-hydroxy-5-methoxyphenyl-1-yl)-aminoquinolin-6-yl]-S-methylsulphoximide 
• 1161837-81-5 S-[4-(3-hydroxy-5-methoxyphenyl-1-yl)-aminoquinolin-6-yl]-N-methoxy-carbonyl-S-methylsulphoximide 
• 653604-52-5 6-[N-(3-cyclopentyloxy-5-isopropyloxyphenyl)carbamyl]-2-naphthalenecarbonitrile 
• 653604-51-4 6-[N-(3,5-diisopropyloxyphenyl)carbamyl]-2-naphthalenecarbonitrile 
• 653604-49-0 3-cyclopentyloxy-5-isopropyloxyaniline 
• 83015-22-9 3,5-diisopropyloxyaniline 
• 653604-48-9 3-amino-5-isopropyloxyphenol 
• 905931-36-4 C₁₃H₈⁽²⁾H₃IO₂ 
• 905931-35-3 C₇H₃⁽²⁾H₄IO₂ 
• 905931-19-3 1-iodo-3-methoxy-5-phenoxybenzene 

Relevant articles and documents

Genetically encoded cleavable protein photo-cross-linker

We have developed a genetically encoded, selenium-based cleavable photo-cross-linker that allows for the separation of bait and prey proteins after protein photo-cross-linking. We have further demonstrated the efficient capture of the in situ generated selenenic acid on the cleaved prey proteins. Our strategy involves tagging the selenenic acid with an alkyne-containing dimethoxyaniline molecule and subsequently labeling with an azide-bearing fluorophore or biotin probe. This cleavage-and-capture after protein photo-cross-linking strategy allows for the efficient capture of prey proteins that are readily accessible by two-dimensional gel-based proteomics and mass spectrometry analysis.

N-PIPERIDIN-4-YL DERIVATIVES

The invention relates to a N-piperidin-4-yl derivative having the general Formula I or a pharmaceutically acceptable salt thereof, to pharmaceutical compositions comprising the same and to the use of said N-piperidin-4-yl derivatives for the treatment and prevention of endometriosis, for the treatment and prevention of pre-menopausal and peri-menopausal hormone-dependent breast cancer, for contraception, or for the treatment of uterine fibroids or other menstrual-related disorders.

Synthesis of substituted carbazoles, indoles, and dibenzofurans by vinylic to aryl palladium migration

Substituted carbazoles, indoles, and dibenzofurans are readily prepared in moderate to excellent yields by the palladium-catalyzed cross-coupling of alkynes and appropriately substituted aryl iodides. This process proceeds by carbopalladation of the alkyn