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
| Molecular Formula | C7H7NO3 |
| Molecular Weight | 153.1354 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Parallel solid-phase synthesis and evaluation of inhibitors of Streptomyces coelicolor type II dehydroquinase. | 2003 Dec 18 |
|
| Synthesis of oligonucleotide containing 4'-o-nitrobenzyloxythymidine and its reactivity. | 2004 |
|
| Isotope effects in photochemistry. 1. o-nitrobenzyl alcohol derivatives. | 2004 Jun 16 |
|
| Amine modification reaction of C4'-oxidized abasic site generated from its caged precursors. | 2005 |
|
| Photochemical reaction mechanisms of 2-nitrobenzyl compounds: 2-nitrobenzyl alcohols form 2-nitroso hydrates by dual proton transfer. | 2005 Jan |
|
| Effects of 4,5-dimethoxy groups on the time-resolved photoconversion of 2-nitrobenzyl alcohols and 2-nitrobenzaldehyde into nitroso derivatives. | 2005 Oct |
|
| Photochemical generation of oligodeoxynucleotide containing a C4'-oxidized abasic site and its efficient amine modification: dependence on structure and microenvironment. | 2008 Jan 4 |
|
| 2-Nitro-benzyl 2-chloro-acetate. | 2009 Sep 5 |
|
| Synthesis of photodegradable hydrogels as dynamically tunable cell culture platforms. | 2010 Dec |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:40:08 GMT 2023
by
admin
on
Fri Dec 15 16:40:08 GMT 2023
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| Record UNII |
5M66390M78
|
| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID40210101
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5M66390M78
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612-25-9
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210-302-6
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