Lithium 3-fluoropyridine-2-carboxylate - CAS 603310-20-9
Catalog: |
BB030658 |
Product Name: |
Lithium 3-fluoropyridine-2-carboxylate |
CAS: |
603310-20-9 |
Synonyms: |
lithium;3-fluoropyridine-2-carboxylate |
IUPAC Name: | lithium;3-fluoropyridine-2-carboxylate |
Description: | Lithium 3-fluoropyridine-2-carboxylate (CAS# 603310-20-9 ) is a useful research chemical. |
Molecular Weight: | 147.03 |
Molecular Formula: | C6H3LiFNO2 |
Canonical SMILES: | [Li+].C1=CC(=C(N=C1)C(=O)[O-])F |
InChI: | InChI=1S/C6H4FNO2.Li/c7-4-2-1-3-8-5(4)6(9)10;/h1-3H,(H,9,10);/q;+1/p-1 |
InChI Key: | POYLONJDIWUFHZ-UHFFFAOYSA-M |
Boiling Point: | 265.2 °C at 760 mmHg |
Appearance: | Off-white to tan powder or crystals |
LogP: | -0.41580 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113224386-A | Cobalt acid lithium battery electrolyte additive, electrolyte and battery thereof | 20210430 |
JP-2012025887-A | Process for producing poly (3-substituted thiophene) | 20100726 |
CA-2794952-A1 | Compounds and method for treatment of hiv | 20100401 |
CA-2794952-C | Compounds and method for treatment of hiv | 20100401 |
CA-2999435-A1 | Compounds and method for treatment of hiv | 20100401 |
Complexity: | 145 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 2 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 147.03078493 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 147.03078493 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 53 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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