Home Aldehydes Benzaldehyde, 3,5-dinitro-

Benzaldehyde, 3,5-dinitro-

CAS No.:
14193-18-1
Catalog Number:
AG001HEN
Molecular Formula:
C7H4N2O5
Molecular Weight:
196.1171
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
250mg
95%
1 week
United States
$269
- +
1g
95%
1 week
United States
$498
- +
5g
95%
1 week
United States
$1134
- +
Product Description
Catalog Number:
AG001HEN
Chemical Name:
Benzaldehyde, 3,5-dinitro-
CAS Number:
14193-18-1
Molecular Formula:
C7H4N2O5
Molecular Weight:
196.1171
MDL Number:
MFCD04971227
IUPAC Name:
3,5-dinitrobenzaldehyde
InChI:
InChI=1S/C7H4N2O5/c10-4-5-1-6(8(11)12)3-7(2-5)9(13)14/h1-4H
InChI Key:
YCTNWTBGSOCMRO-UHFFFAOYSA-N
SMILES:
O=Cc1cc(cc(c1)[N+](=O)[O-])[N+](=O)[O-]
Properties
Complexity:
234  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
196.012g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
196.118g/mol
Monoisotopic Mass:
196.012g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
109A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.2  
Literature
Title Journal
Focused review: agmatine in fermented foods. Frontiers in microbiology 20120101
Study of stereoselective interactions of carbamoylated quinine and quinidine with 3,5-dinitrobenzoyl α-amino acids using VCD spectroscopy in the region of C−H stretching vibrations. Chirality 20110401
Polyamines in foods: development of a food database. Food & nutrition research 20110101
A 3,5-dinitro-benzoyl derivative of a stereoisomer of glycerol menthonide. Acta crystallographica. Section E, Structure reports online 20090701
(1RS,4RS,5RS)-Methyl 2-(3,5-dinitro-benzo-yl)-2-oxa-3-aza-bicyclo-[3.3.0]oct-7-ene-4-carboxyl-ate. Acta crystallographica. Section E, Structure reports online 20090501
Pi-Pi complexation of bupivacaine and analogues with aromatic receptors: implications for overdose remediation. International journal of nanomedicine 20070901
Preparation of a mercaptopropyl bonded silica intermediate in supercritical carbon dioxide: synthesis, characterisation and chromatography of a quinine based chiral stationary phase. Journal of chromatography. A 20070713
[Preparation and evaluation of 3,5-dinitrobenzoyl-bonded silica gel stationary phase for high performance liquid chromatography]. Se pu = Chinese journal of chromatography 20050301
Efficient resolution of racemic 1,1'-bi-2-naphthol with chiral selectors identified from a small library. Journal of chromatography. A 20050107
Determination of azide as the 3,5-dinitrobenzoyl derivative by capillary electrophoresis. Journal of chromatography. A 20040806
Retention of 3,5-dinitrobenzoyl derivatives of linear alcohol polyethoxylates in reversed-phase liquid chromatographic system with acetonitrile-water mobile phase. Journal of chromatography. A 20031222
Micro-HPLC and standard-size HPLC for the separation of peptide stereoisomers employing an ion-exchange principle. Journal of pharmaceutical and biomedical analysis 20030115
Enantiomeric separation of diuretics on a novel Pirkle-type chiral stationary phase. Biomedical chromatography : BMC 20021001
Enantiomeric separation of N-protected amino acids by non-aqueous capillary electrophoresis with dimeric forms of quinine and quinidine derivatives serving as chiral selectors. Journal of chromatography. A 20020301
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
Synthesis of branched polysaccharides by polymerization of 6-O-t-butyldimethylsilyl-D-glucal through stereoregular haloglycosylation. Carbohydrate letters 20010101
Immobilization of difunctional building blocks on hydroxysuccinimide activated silica: versatile in situ preparation of chiral stationary phases. Chirality 20010101
Properties