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[ CAS No. 165547-79-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 165547-79-5
Chemical Structure| 165547-79-5
Structure of 165547-79-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 165547-79-5 ]

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Product Details of [ 165547-79-5 ]

CAS No. :165547-79-5 MDL No. :MFCD09701353
Formula : C5H3ClN2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :UKIZCTHOMJXNIX-UHFFFAOYSA-N
M.W : 174.54 Pubchem ID :519282
Synonyms :

Calculated chemistry of [ 165547-79-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 40.09
TPSA : 78.94 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.06 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.74
Log Po/w (XLOGP3) : 1.84
Log Po/w (WLOGP) : 1.35
Log Po/w (MLOGP) : 0.52
Log Po/w (SILICOS-IT) : -0.53
Consensus Log Po/w : 0.78

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.42
Solubility : 0.665 mg/ml ; 0.00381 mol/l
Class : Soluble
Log S (Ali) : -3.12
Solubility : 0.133 mg/ml ; 0.000762 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.44
Solubility : 6.29 mg/ml ; 0.0361 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.88

Safety of [ 165547-79-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 165547-79-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 165547-79-5 ]

[ 165547-79-5 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 165547-79-5 ]
  • [ 100-39-0 ]
  • [ 219735-84-9 ]
YieldReaction ConditionsOperation in experiment
84% With silver carbonate; In benzene; at 20℃; for 72h; 2-(benzyloxy)-4-chloro-3-nitropyridine. A mixture of 4-chloro-3-nitro-2-pyridine (4.0 g, 22.9 mmol), benzylbromide (3.3 mL, 27.5 mmol), and silver carbonate (7.6 g, 27.5 mmol) in benzene (80 mL) was added to a round bottom flask. The flask was wrapped in aluminum foil to keep the reaction in the dark and stirred at room temperature. After 3 days, the mixture was filtered through celite; the celite was washed with benzene and methanol. The filtrate and washings were combined, concentrated, and chromatographed on silica gel (0%-30% ethyl acetate:hexane gradient as the eluent) to yield the benzylated product. 5.1 g (84%). HPLC (method A): Rt=10.3 min. MS: [M+H]+=265.
  • 2
  • 3-nitro-pyridine-2,4-diol; compound with cycloheptylamine [ No CAS ]
  • [ 165547-79-5 ]
  • 3
  • [ 165547-79-5 ]
  • [ 514206-38-3 ]
  • 4
  • [ 165547-79-5 ]
  • [ 514206-34-9 ]
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Technical Information

? Alkyl Halide Occurrence ? Appel Reaction ? Baeyer-Villiger Oxidation ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Bucherer-Bergs Reaction ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Chugaev Reaction ? Clemmensen Reduction ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Corey-Kim Oxidation ? Dess-Martin Oxidation ? Fischer Indole Synthesis ? General Reactivity ? Grignard Reaction ? Henry Nitroaldol Reaction ? Hiyama Cross-Coupling Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Jones Oxidation ? Kinetics of Alkyl Halides ? Kumada Cross-Coupling Reaction ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? Martin's Sulfurane Dehydrating Reagent ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mitsunobu Reaction ? Moffatt Oxidation ? Oxidation of Alcohols by DMSO ? Passerini Reaction ? Paternò-Büchi Reaction ? Petasis Reaction ? Peterson Olefination ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Alcohols ? Preparation of Aldehydes and Ketones ? Preparation of Amines ? Prins Reaction ? Reactions of Alcohols ? Reactions of Aldehydes and Ketones ? Reactions of Alkyl Halides with Reducing Metals ? Reactions of Amines ? Reactions with Organometallic Reagents ? Reformatsky Reaction ? Ritter Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Sharpless Olefin Synthesis ? Specialized Acylation Reagents-Ketenes ? Stille Coupling ? Stobbe Condensation ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling ? Swern Oxidation ? Tebbe Olefination ? Ugi Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
Historical Records

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