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[ CAS No. 104222-34-6 ] {[proInfo.proName]}

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Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 104222-34-6
Chemical Structure| 104222-34-6
Structure of 104222-34-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 104222-34-6 ]

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Product Citations

Product Details of [ 104222-34-6 ]

CAS No. :104222-34-6 MDL No. :MFCD00052698
Formula : C6H4ClFN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :VRJKEIWZSOHDOH-UHFFFAOYSA-N
M.W : 190.56 Pubchem ID :517835
Synonyms :

Calculated chemistry of [ 104222-34-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 44.64
TPSA : 71.84 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.79 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.2
Log Po/w (XLOGP3) : 2.35
Log Po/w (WLOGP) : 2.4
Log Po/w (MLOGP) : 1.32
Log Po/w (SILICOS-IT) : 0.08
Consensus Log Po/w : 1.47

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.81
Solubility : 0.298 mg/ml ; 0.00156 mol/l
Class : Soluble
Log S (Ali) : -3.5
Solubility : 0.0605 mg/ml ; 0.000317 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.32
Solubility : 0.918 mg/ml ; 0.00482 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.06

Safety of [ 104222-34-6 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P280-P301+P310-P311 UN#:2811
Hazard Statements:H301+H311+H331 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 104222-34-6 ]

* 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.

  • Upstream synthesis route of [ 104222-34-6 ]

[ 104222-34-6 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 81962-58-5 ]
  • [ 104222-34-6 ]
Reference: [1] Heterocycles, 1995, vol. 41, # 10, p. 2203 - 2220
[2] Patent: US4826982, 1989, A,
[3] Heterocycles, 2016, vol. 92, # 7, p. 1282 - 1292
[4] European Journal of Medicinal Chemistry, 2016, vol. 117, p. 230 - 240
  • 2
  • [ 367-21-5 ]
  • [ 104222-34-6 ]
Reference: [1] Heterocycles, 1995, vol. 41, # 10, p. 2203 - 2220
[2] Heterocycles, 2016, vol. 92, # 7, p. 1282 - 1292
[3] European Journal of Medicinal Chemistry, 2016, vol. 117, p. 230 - 240
  • 3
  • [ 877-90-7 ]
  • [ 104222-34-6 ]
Reference: [1] Heterocycles, 1995, vol. 41, # 10, p. 2203 - 2220
[2] Heterocycles, 2016, vol. 92, # 7, p. 1282 - 1292
[3] European Journal of Medicinal Chemistry, 2016, vol. 117, p. 230 - 240
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Technical Information

? Acyl Group Substitution ? Alkyl Halide Occurrence ? Appel Reaction ? Arndt-Eistert Homologation ? Baeyer-Villiger Oxidation ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Chan-Lam Coupling Reaction ? Chugaev Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Corey-Kim Oxidation ? Dess-Martin Oxidation ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? General Reactivity ? Grignard Reaction ? Henry Nitroaldol Reaction ? Hiyama Cross-Coupling Reaction ? Horner-Wadsworth-Emmons Reaction ? Hunsdiecker-Borodin Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Jones Oxidation ? Kinetics of Alkyl Halides ? Kumada Cross-Coupling Reaction ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? Mannich Reaction ? Martin's Sulfurane Dehydrating Reagent ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mitsunobu Reaction ? Moffatt Oxidation ? Nomenclature of Ethers ? 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 Alkylbenzene ? Preparation of Amines ? Preparation of Carboxylic Acids ? Preparation of Ethers ? Prins Reaction ? Reactions of Alcohols ? Reactions of Aldehydes and Ketones ? Reactions of Alkyl Halides with Reducing Metals ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions of Carboxylic Acids ? Reactions of Ethers ? Reactions with Organometallic Reagents ? Reformatsky Reaction ? Ritter Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Sharpless Olefin Synthesis ? Specialized Acylation Reagents-Carbodiimides and Related Reagents ? Specialized Acylation Reagents-Ketenes ? Specialized Acylation Reagents-Vilsmeier Reagent ? Stille Coupling ? Stobbe Condensation ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling ? Swern Oxidation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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