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612-25-9

612-25-9 | Benzenemethanol, nitro-

CAS No: 612-25-9 Catalog No: AG00IATJ MDL No:MFCD00007186

Product Description

Catalog Number:
AG00IATJ
Chemical Name:
Benzenemethanol, nitro-
CAS Number:
612-25-9
Molecular Formula:
C7H7NO3
Molecular Weight:
153.1354
MDL Number:
MFCD00007186
IUPAC Name:
(2-nitrophenyl)methanol
InChI:
InChI=1S/C7H7NO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-4,9H,5H2
InChI Key:
BWRBVBFLFQKBPT-UHFFFAOYSA-N
SMILES:
OCc1ccccc1[N+](=O)[O-]
EC Number:
210-302-6
UNII:
5M66390M78
NSC Number:
66512

Properties

Complexity:
143  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
153.043g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
153.137g/mol
Monoisotopic Mass:
153.043g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
66A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.2  

Literature

Title Journal
Stereochemistry of benzylic carbon substitution coupled with ring modification of 2-nitrobenzyl groups as key determinants for fast-cleaving reversible terminators. Angewandte Chemie (International ed. in English) 20120213
Debundling, selection and release of SWNTs using fluorene-based photocleavable polymers. Chemical communications (Cambridge, England) 20110714
Light-triggered covalent assembly of gold nanoparticles in aqueous solution. Chemical communications (Cambridge, England) 20110407
Synthesis of photodegradable hydrogels as dynamically tunable cell culture platforms. Nature protocols 20101201
2-Nitro-benzyl 2-chloro-acetate. Acta crystallographica. Section E, Structure reports online 20091001
Photochemical generation of oligodeoxynucleotide containing a C4'-oxidized abasic site and its efficient amine modification: dependence on structure and microenvironment. The Journal of organic chemistry 20080104
Effects of 4,5-dimethoxy groups on the time-resolved photoconversion of 2-nitrobenzyl alcohols and 2-nitrobenzaldehyde into nitroso derivatives. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20051001
Photochemical reaction mechanisms of 2-nitrobenzyl compounds: 2-nitrobenzyl alcohols form 2-nitroso hydrates by dual proton transfer. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20050101
Amine modification reaction of C4'-oxidized abasic site generated from its caged precursors. Nucleic acids symposium series (2004) 20050101
Isotope effects in photochemistry. 1. o-nitrobenzyl alcohol derivatives. Journal of the American Chemical Society 20040616
Synthesis of oligonucleotide containing 4'-o-nitrobenzyloxythymidine and its reactivity. Nucleic acids symposium series (2004) 20040101
Parallel solid-phase synthesis and evaluation of inhibitors of Streptomyces coelicolor type II dehydroquinase. Journal of medicinal chemistry 20031218

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