3-Nitro-1H-indole - CAS 4770-03-0
Catalog: |
BB026364 |
Product Name: |
3-Nitro-1H-indole |
CAS: |
4770-03-0 |
Synonyms: |
3-nitro-1H-indole; 3-nitro-1H-indole |
IUPAC Name: | 3-nitro-1H-indole |
Description: | 3-Nitro-1H-indole (CAS# 4770-03-0) is a useful research chemical. |
Molecular Weight: | 162.15 |
Molecular Formula: | C8H6N2O2 |
Canonical SMILES: | C1=CC=C2C(=C1)C(=CN2)[N+](=O)[O-] |
InChI: | InChI=1S/C8H6N2O2/c11-10(12)8-5-9-7-4-2-1-3-6(7)8/h1-5,9H |
InChI Key: | LSMXNZJFLGIPMS-UHFFFAOYSA-N |
LogP: | 2.59930 |
Publication Number | Title | Priority Date |
CN-113461590-A | Method for constructing 1-substituted cyclopropane compound by virtue of phosphine-catalyzed C-H activated amination reaction of cyclopropane | 20210615 |
US-2021301329-A1 | Single Cell Genetic Analysis | 20200324 |
WO-2021194699-A1 | Single cell genetic analysis | 20200324 |
US-2021285044-A1 | Systems and methods for nucleic acid processing using degenerate nucleotides | 20200313 |
WO-2021173721-A1 | Selective androgen receptor degrader (sard) ligands and methods of use thereof | 20200225 |
PMID | Publication Date | Title | Journal |
17880093 | 20071011 | Multicomponent domino [4+2]/[3+2] cycloadditions of nitroheteroaromatics: an efficient synthesis of fused nitrogenated polycycles | Organic letters |
16170793 | 20051101 | Catalytic enantioselective addition of indoles to arylnitroalkenes: an effective route to enantiomerically enriched tryptamine precursors | Chirality |
Complexity: | 190 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 162.042927438 |
Formal Charge: | 0 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 162.042927438 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 61.6 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.4 |
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