Home Other Building Blocks 2-Acetamidophenol

2-Acetamidophenol

CAS No.:
614-80-2
Catalog Number:
AG003GAL
Molecular Formula:
C8H9NO2
Molecular Weight:
151.1626
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$33
- +
25g
95%
In Stock USA
United States
$54
- +
100g
95%
In Stock USA
United States
$105
- +
500g
95%
In Stock USA
United States
$362
- +
Product Description
Catalog Number:
AG003GAL
Chemical Name:
2-Acetamidophenol
CAS Number:
614-80-2
Molecular Formula:
C8H9NO2
Molecular Weight:
151.1626
MDL Number:
MFCD00002181
IUPAC Name:
N-(2-hydroxyphenyl)acetamide
InChI:
InChI=1S/C8H9NO2/c1-6(10)9-7-4-2-3-5-8(7)11/h2-5,11H,1H3,(H,9,10)
InChI Key:
ADVGKWPZRIDURE-UHFFFAOYSA-N
SMILES:
CC(=O)Nc1ccccc1O
EC Number:
210-396-9
UNII:
4AS8989RNI
NSC Number:
3989
Properties
Complexity:
147  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
151.063g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
151.165g/mol
Monoisotopic Mass:
151.063g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
49.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.7  
Literature
Title Journal
Acetaminophen-induced differentiation of human breast cancer stem cells and inhibition of tumor xenograft growth in mice. Biochemical pharmacology 20110501
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
N-(2-hydroxy phenyl) acetamide inhibits inflammation-related cytokines and ROS in adjuvant-induced arthritic (AIA) rats. International immunopharmacology 20100801
Hydroxyl-functionalized polyaniline nanospheres: tracing molecular interactions at the nanosurface via vitamin C sensing. Langmuir : the ACS journal of surfaces and colloids 20080902
Interactions of Bacillus mojavensis and Fusarium verticillioides with a benzoxazolinone (BOA) and its transformation product, APO. Journal of chemical ecology 20071001
Zea mays: benzoxazolinone detoxification under sulfur deficiency conditions--a complex allelopathic alliance including endophytic Fusarium verticillioides. Journal of chemical ecology 20070201
Amorphane sesquiterpenes from a marine Streptomyces sp. Journal of natural products 20070201
Microsphere-based protease assays and screening application for lethal factor and factor Xa. Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501
Joint action of benzoxazinone derivatives and phenolic acids. Journal of agricultural and food chemistry 20060222
Method for screening and quantitative determination of serum levels of salicylic Acid, acetaminophen, theophylline, phenobarbital, bromvalerylurea, pentobarbital, and amobarbital using liquid chromatography/electrospray mass spectrometry. Biological & pharmaceutical bulletin 20060101
Application of stable isotope labeled glutathione and rapid scanning mass spectrometers in detecting and characterizing reactive metabolites. Rapid communications in mass spectrometry : RCM 20050101
Analysis of paraquat, diquat and two diquat metabolites in biological materials by high-performance liquid chromatography. Legal medicine (Tokyo, Japan) 20020901
Hydroxylated 2-amino-3H-phenoxazin-3-one derivatives as products of 2-hydroxy-1,4-benzoxazin-3-one (HBOA) biotransformation by Chaetosphaeria sp., an endophytic fungus from Aphelandra tetragona. Zeitschrift fur Naturforschung. C, Journal of biosciences 20020101
Properties