Home Nitros 3,5-Dinitrobenzamide

3,5-Dinitrobenzamide

CAS No.:
121-81-3
Catalog Number:
AG003IPF
Molecular Formula:
C7H5N3O5
Molecular Weight:
211.1317
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$13
- +
5g
95%
In Stock USA
United States
$24
- +
Product Description
Catalog Number:
AG003IPF
Chemical Name:
3,5-Dinitrobenzamide
CAS Number:
121-81-3
Molecular Formula:
C7H5N3O5
Molecular Weight:
211.1317
MDL Number:
MFCD00007985
IUPAC Name:
3,5-dinitrobenzamide
InChI:
InChI=1S/C7H5N3O5/c8-7(11)4-1-5(9(12)13)3-6(2-4)10(14)15/h1-3H,(H2,8,11)
InChI Key:
UUKWKUSGGZNXGA-UHFFFAOYSA-N
SMILES:
NC(=O)c1cc(cc(c1)[N+](=O)[O-])[N+](=O)[O-]
EC Number:
204-499-8
UNII:
9DUJ3CMK8S
Properties
Complexity:
272  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
211.023g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
211.133g/mol
Monoisotopic Mass:
211.023g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
135A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.8  
Literature
Title Journal
Highly sensitive voltammetric sensor based on catechol-derivative-multiwall carbon nanotubes for the catalytic determination of captopril in patient human urine samples. Colloids and surfaces. B, Biointerfaces 20111015
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
Charge-transfer interaction between poly(9-vinylcarbazole) and 3,5-dinitrobenzamido group or 3-nitrobenzamido group. Langmuir : the ACS journal of surfaces and colloids 20100302
Preparative enantioseparation of (+/-)-N-(3,4-cis-3-decyl-1,2,3,4-tetrahydrophenanthren-4-yl)-3,5-dinitrobenzamide by centrifugal partition chromatography. Journal of chromatography. A 20100219
Continuous separation of racemic 3,5-dinitrobenzoyl-amino acids in a centrifugal contact separator with the aid of cinchona-based chiral host compounds. Chemistry (Weinheim an der Bergstrasse, Germany) 20090101
Discrimination of enantiomers of alpha-amino acids by chiral derivatizing reagents from trans-1,2-diaminocyclohexane. Chirality 20080301
Pi-Pi complexation of bupivacaine and analogues with aromatic receptors: implications for overdose remediation. International journal of nanomedicine 20070901
A comprehensive chemoselective and enantioselective 2D-HPLC set-up for fast enantiomer analysis of a multicomponent mixture of derivatized amino acids. Analytical and bioanalytical chemistry 20070801
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
Determination of enantiomeric composition by negative-ion electrospray ionization-mass spectrometry using deprotonated N-(3,5-dinitrobenzoyl)amino acids as chiral selectors. Chirality 20051001
PnrA, a new nitroreductase-family enzyme in the TNT-degrading strain Pseudomonas putida JLR11. Environmental microbiology 20050801
Elucidation of the chiral recognition mechanism of cinchona alkaloid carbamate-type receptors for 3,5-dinitrobenzoyl amino acids. Journal of the American Chemical Society 20020724
Solid-phase synthesis of chiral stationary phases based on 2,4,5,6-tetrachloro-1,3-dicyanobenzene derivatives spaced from N-3,5-dinitrobenzoyl alpha-amino acids: comparative study of their resolution efficacy. Chirality 20010601
Efficacy of 101 antimicrobials and other agents on the development of Cryptosporidium parvum in vitro. Annals of tropical medicine and parasitology 19961201
Properties