Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H7NO3 |
Molecular Weight | 153.1354 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OCC1=CC=CC=C1[N+]([O-])=O
InChI
InChIKey=BWRBVBFLFQKBPT-UHFFFAOYSA-N
InChI=1S/C7H7NO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-4,9H,5H2
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Parallel solid-phase synthesis and evaluation of inhibitors of Streptomyces coelicolor type II dehydroquinase. | 2003 Dec 18 |
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Synthesis of oligonucleotide containing 4'-o-nitrobenzyloxythymidine and its reactivity. | 2004 |
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Amine modification reaction of C4'-oxidized abasic site generated from its caged precursors. | 2005 |
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Photochemical generation of oligodeoxynucleotide containing a C4'-oxidized abasic site and its efficient amine modification: dependence on structure and microenvironment. | 2008 Jan 4 |
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2-Nitro-benzyl 2-chloro-acetate. | 2009 Sep 5 |
|
Synthesis of photodegradable hydrogels as dynamically tunable cell culture platforms. | 2010 Dec |
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66512
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DTXSID40210101
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5M66390M78
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11923
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612-25-9
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210-302-6
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SUBSTANCE RECORD