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[ CAS No. 2011-66-7 ] {[proInfo.proName]}

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Chemical Structure| 2011-66-7
Chemical Structure| 2011-66-7
Structure of 2011-66-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2011-66-7 ]

CAS No. :2011-66-7 MDL No. :MFCD00792453
Formula : C13H9ClN2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :GRDGBWVSVMLKBV-UHFFFAOYSA-N
M.W : 276.68 Pubchem ID :74830
Synonyms :
Chemical Name :(2-Amino-5-nitrophenyl)(2-chlorophenyl)methanone

Calculated chemistry of [ 2011-66-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 74.55
TPSA : 88.91 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -5.44 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.65
Log Po/w (XLOGP3) : 3.59
Log Po/w (WLOGP) : 3.07
Log Po/w (MLOGP) : 1.79
Log Po/w (SILICOS-IT) : 1.11
Consensus Log Po/w : 2.24

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.09
Solubility : 0.0227 mg/ml ; 0.0000819 mol/l
Class : Moderately soluble
Log S (Ali) : -5.14
Solubility : 0.00199 mg/ml ; 0.00000718 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.5
Solubility : 0.00877 mg/ml ; 0.0000317 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 1.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.36

Safety of [ 2011-66-7 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P201-P308+P313 UN#:N/A
Hazard Statements:H341 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 2011-66-7 ]

* 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 [ 2011-66-7 ]

[ 2011-66-7 ] Synthesis Path-Downstream   1~5

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  • 4
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YieldReaction ConditionsOperation in experiment
With hydrogenchloride;copper(I) chloride; In water; acetic acid; sodium nitrite; EXAMPLE 26 (2-Chloro-5-nitrophenyl)(2-chlorophenyl)methanone To 180 ml of concentrated sulfuric acid cooled to 0 in an ice bath was added 28 g (0.4 mol) of sodium nitrite in portions at such a rate that the temperature did not go above 10. This mixture was warmed on a steam bath until a solution formed. It was then cooled to 30 and a solution of 110.68 g (0.4 mol) of <strong>[2011-66-7]2-amino-5-nitro-2'-chlorobenzophenone</strong> in 300 mL of hot acetic acid was added at such a rate that the temperature did not exceed 40. This mixture was stirred without heating for 2.5 hr, and then poured slowly into a mixture of 800 mL of concentrated hydrochloric acid and 80 g of cuprous chloride. This mixture was heated to 80 on a steam bath for 40 min until the foaming had subsided, poured into 2 l of water, and allowed to stand overnight. The solid was collected, washed with water and recrystallized from methanol to give product, mp 76-79. An analytical sample prepared by recrystallization from methanol had mp 78.5-80.
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Technical Information

? Alkyl Halide Occurrence ? 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 ? Clemmensen Reduction ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? General Reactivity ? Grignard Reaction ? Henry Nitroaldol Reaction ? Hiyama Cross-Coupling Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Kinetics of Alkyl Halides ? Kumada Cross-Coupling Reaction ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? Mannich Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Passerini Reaction ? Paternò-Büchi Reaction ? Petasis Reaction ? Peterson Olefination ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Alkyl Halides with Reducing Metals ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reformatsky Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Specialized Acylation Reagents-Ketenes ? Specialized Acylation Reagents-Vilsmeier Reagent ? Stille Coupling ? Stobbe Condensation ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
Historical Records

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