Home Nitros 2-Methyl-6-nitrobenzoic anhydride

2-Methyl-6-nitrobenzoic anhydride

CAS No.:
434935-69-0
Catalog Number:
AG003HO3
Molecular Formula:
C16H12N2O7
Molecular Weight:
344.2757
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
97%
In Stock USA
United States
$44
- +
5g
97%
In Stock USA
United States
$132
- +
10g
97%
In Stock USA
United States
$219
- +
25g
97%
In Stock USA
United States
$438
- +
100g
97%
In Stock USA
United States
$1313
- +
Product Description
Catalog Number:
AG003HO3
Chemical Name:
2-Methyl-6-nitrobenzoic anhydride
CAS Number:
434935-69-0
Molecular Formula:
C16H12N2O7
Molecular Weight:
344.2757
MDL Number:
MFCD06797117
IUPAC Name:
(2-methyl-6-nitrobenzoyl) 2-methyl-6-nitrobenzoate
InChI:
InChI=1S/C16H12N2O7/c1-9-5-3-7-11(17(21)22)13(9)15(19)25-16(20)14-10(2)6-4-8-12(14)18(23)24/h3-8H,1-2H3
InChI Key:
YEKPNMQQSPHKBP-UHFFFAOYSA-N
SMILES:
O=C(c1c(C)cccc1[N+](=O)[O-])OC(=O)c1c(C)cccc1[N+](=O)[O-]
Properties
Complexity:
506  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
344.064g/mol
Formal Charge:
0
Heavy Atom Count:
25  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
344.279g/mol
Monoisotopic Mass:
344.064g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
135A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.6  
Literature
Title Journal
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MNBA-mediated β-lactone formation: mechanistic studies and application for the asymmetric total synthesis of tetrahydrolipstatin. The Journal of organic chemistry 20120601
Two antimycin A analogues from marine-derived actinomycete Streptomyces lusitanus. Marine drugs 20120301
Total synthesis of cyanolide A and confirmation of its absolute configuration. Organic letters 20100618
Fusaric acid as a novel proton-affinitive derivatizing reagent for highly sensitive quantification of hydroxysteroids by LC-ESI-MS/MS. Journal of the American Society for Mass Spectrometry 20100201
Antineoplastic agents. 571. Total synthesis of bacillistatin 2. Journal of natural products 20090327
Evaluation of the efficiency of the macrolactonization using MNBA in the synthesis of erythromycin A aglycon. Chemical record (New York, N.Y.) 20090101
Simultaneous determination of tetrahydrocortisol, allotetrahydrocortisol and tetrahydrocortisone in human urine by liquid chromatography-electrospray ionization tandem mass spectrometry. Steroids 20080801
Development of sensitive derivatization method for aldosterone in liquid chromatography-electrospray ionization tandem mass spectrometry of corticosteroids. Journal of chromatography. A 20080725
Total synthesis of 2-hydroxytetracosanolide and 2-hydroxy-24-oxooctacosanolide by using an effective lactonization. Chemistry, an Asian journal 20080201
4-(Dimethylamino)pyridine N-oxide (DMAPO): an effective nucleophilic catalyst in the peptide coupling reaction with 2-methyl-6-nitrobenzoic anhydride. Chemistry, an Asian journal 20080201
Use of novel picolinoyl derivatization for simultaneous quantification of six corticosteroids by liquid chromatography-electrospray ionization tandem mass spectrometry. Journal of chromatography. A 20071130
Highly sensitive determination of estrone and estradiol in human serum by liquid chromatography-electrospray ionization tandem mass spectrometry. Steroids 20071001
Synthesis of pyridine-carboxylate derivatives of hydroxysteroids for liquid chromatography-electrospray ionization-mass spectrometry. Steroids 20070101
Stereoselective total synthesis of the proposed structure of 2-epibotcinolide. Organic letters 20061109
The first total synthesis of (-) and (+)-2-hydroxy-24-oxooctacosanolide using an effective lactonization. Organic letters 20061012
Enantioselective total synthesis of octalactin a using asymmetric aldol reactions and a rapid lactonization to form a medium-sized ring. Chemistry (Weinheim an der Bergstrasse, Germany) 20051104
An effective use of benzoic anhydride and its derivatives for the synthesis of carboxylic esters and lactones: a powerful and convenient mixed anhydride method promoted by basic catalysts. The Journal of organic chemistry 20040319
Properties