Home Other Building Blocks Carbamic acid, N-phenyl-, 1-methylethyl ester

Carbamic acid, N-phenyl-, 1-methylethyl ester

CAS No.:
122-42-9
Catalog Number:
AG0016JC
Molecular Formula:
C10H13NO2
Molecular Weight:
179.2157
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
25mg
>98%(GC)powder
In Stock USA
United States
$73
- +
100mg
>98%(GC)powder
In Stock USA
United States
$156
- +
Product Description
Catalog Number:
AG0016JC
Chemical Name:
Carbamic acid, N-phenyl-, 1-methylethyl ester
CAS Number:
122-42-9
Molecular Formula:
C10H13NO2
Molecular Weight:
179.2157
MDL Number:
MFCD00026382
IUPAC Name:
propan-2-yl N-phenylcarbamate
InChI:
InChI=1S/C10H13NO2/c1-8(2)13-10(12)11-9-6-4-3-5-7-9/h3-8H,1-2H3,(H,11,12)
InChI Key:
VXPLXMJHHKHSOA-UHFFFAOYSA-N
SMILES:
CC(OC(=O)Nc1ccccc1)C
EC Number:
204-542-0
UNII:
Y647G714RY
NSC Number:
2105
Properties
Complexity:
162  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
179.095g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
179.219g/mol
Monoisotopic Mass:
179.095g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
38.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.6  
Literature
Title Journal
[Determination of 88 pesticide residues in cranberry plant extract by gas chromatography-triple quadrupole tandem mass spectrometry]. Se pu = Chinese journal of chromatography 20111001
Mining biologically-active molecules for inhibitors of fatty acid amide hydrolase (FAAH): identification of phenmedipham and amperozide as FAAH inhibitors. Bioorganic & medicinal chemistry letters 20091201
Removal of propham from water by using electro-Fenton technology: kinetics and mechanism. Chemosphere 20081001
Effects of the herbicide isopropyl-N-phenyl carbamate on microtubules and MTOCs in lines of Nicotiana sylvestris resistant and sensitive to its action. Cell biology international 20080601
Propham mineralization in aqueous medium by anodic oxidation using boron-doped diamond anode: influence of experimental parameters on degradation kinetics and mineralization efficiency. Water research 20080601
Determination of plant resistance to carbamate herbicidal compounds inhibiting cell division and early growth by seed and plantlets bioassays. Nature protocols 20060101
Heterogeneous photocatalysed reaction of three selected pesticide derivatives, propham, propachlor and tebuthiuron in aqueous suspensions of titanium dioxide. Chemosphere 20051001
Determination of imidacloprid, metalaxyl, myclobutanil, propham, and thiabendazole in fruits and vegetables by liquid chromatography-atmospheric pressure chemical ionization-mass spectrometry. Fresenius' journal of analytical chemistry 20010901
Properties