3-Nitro-2-pyridinesulfenyl chloride - CAS 68206-45-1
Catalog: |
BB033492 |
Product Name: |
3-Nitro-2-pyridinesulfenyl chloride |
CAS: |
68206-45-1 |
Synonyms: |
(3-nitropyridin-2-yl) thiohypochlorite |
IUPAC Name: | (3-nitropyridin-2-yl) thiohypochlorite |
Description: | 3-Nitro-2-pyridinesulfenyl chloride (CAS# 68206-45-1) is a useful research chemical. |
Molecular Weight: | 190.61 |
Molecular Formula: | C5H3ClN2O2S |
Canonical SMILES: | C1=CC(=C(N=C1)SCl)[N+](=O)[O-] |
InChI: | InChI=1S/C5H3ClN2O2S/c6-11-5-4(8(9)10)2-1-3-7-5/h1-3H |
InChI Key: | WTKQMHWYSBWUBE-UHFFFAOYSA-N |
Boiling Point: | 376.8 °C at 760 mmHg |
Purity: | 95 % |
Density: | 1.58 g/cm3 |
MDL: | MFCD00274609 |
LogP: | 2.75890 |
GHS Hazard Statement: | H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation] |
Precautionary Statement: | P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-112979759-A | Method for preparing procatide by solid-liquid combination | 20210408 |
CN-111925418-A | Liquid phase synthesis method of ytka peptide | 20200927 |
CN-111925418-B | Liquid phase synthesis method of ytka peptide | 20200927 |
WO-2021203055-A1 | Viral entry inhibitors and rna polymerase inhibitors | 20200403 |
WO-2021202874-A1 | Furin inhibitors for treating coronavirus infections | 20200402 |
PMID | Publication Date | Title | Journal |
19403512 | 20090901 | Cell-surface thiols affect cell entry of disulfide-conjugated peptides | FASEB journal : official publication of the Federation of American Societies for Experimental Biology |
17328865 | 20070420 | C-Npys (S-3-nitro-2-pyridinesulfenyl) and peptide derivatives can inhibit a serine-thiol proteinase activity from Paracoccidioides brasiliensis | Biochemical and biophysical research communications |
16557331 | 20060407 | A novel heterobifunctional linker for facile access to bioconjugates | Organic & biomolecular chemistry |
16248092 | 20050101 | A convenient method for the synthesis of oligonucleotide-cationic peptide conjugates | Nucleosides, nucleotides & nucleic acids |
11694304 | 20011030 | Discriminative disulfide-bonding affinity labeling of opioid receptor subtypes | Journal of biochemical and biophysical methods |
Complexity: | 152 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 189.9603762 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 189.9603762 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 84 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.9 |
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Related Functional Groups
Pyridines
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