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[ CAS No. 20099-90-5 ] {[proInfo.proName]}

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Chemical Structure| 20099-90-5
Chemical Structure| 20099-90-5
Structure of 20099-90-5 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Details of [ 20099-90-5 ]

CAS No. :20099-90-5 MDL No. :MFCD00229872
Formula : C9H7BrO3 Boiling Point : -
Linear Structure Formula :- InChI Key :ZMHLKKVZTJBBHK-UHFFFAOYSA-N
M.W : 243.05 Pubchem ID :2756836
Synonyms :

Calculated chemistry of [ 20099-90-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.11
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 51.47
TPSA : 54.37 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.08 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.13
Log Po/w (XLOGP3) : 2.4
Log Po/w (WLOGP) : 1.96
Log Po/w (MLOGP) : 1.73
Log Po/w (SILICOS-IT) : 2.11
Consensus Log Po/w : 1.87

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -3.0
Solubility : 0.242 mg/ml ; 0.000994 mol/l
Class : Soluble
Log S (Ali) : -3.18
Solubility : 0.159 mg/ml ; 0.000655 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.98
Solubility : 0.253 mg/ml ; 0.00104 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.51

Safety of [ 20099-90-5 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:1759
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 20099-90-5 ]

* 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 [ 20099-90-5 ]

[ 20099-90-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 214834-18-1 ]
  • [ 20099-90-5 ]
  • [ 860344-62-3 ]
YieldReaction ConditionsOperation in experiment
In tetrahydrofuran; at 20 - 80℃; for 2.08333h; 4-Thiocarbamoyl-piperidine-1-carboxylic acid tert-butyl ester (2.47 mmol) and 4- (2- Bromo-acetyl)-benzoic acid (2.47 mmol) were mixed in THF (12 mL). After stirring at room temperature for 5 minutes the mixture was heated to 80 C for 2 hours. The volume was reduced to 5 mL and diethylether (5 mL) was added. The mixture was then cooled to-20 C and filtered. The solid was washed with a small amount of diethylether and dried. m/z = 289.1 in MS ES+, which was characterized by hplc and MS and used in the next step without any further purification.
  • 2
  • [ 20099-90-5 ]
  • [ 42182-27-4 ]
  • 4-(7-Cyanoimidazo[1,2-a]pyridin-2-yl)benzoic acid hydrobromide [ No CAS ]
YieldReaction ConditionsOperation in experiment
In ethanol; Example 5 8.5 g of <strong>[42182-27-4]2-amino-4-cyanopyridine</strong> and 27.5 g of 4-bromoacetylbenzoic acid are boiled in 260 ml of ethanol for 20 h. After cooling, the precipitate is filtered off with suction and subjected to the customary working-up. 4-(7-Cyanoimidazo[1,2-a]pyridin-2-yl)benzoic acid hydrobromide is obtained, m.p. >310°.
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Technical Information

? Alkyl Halide Occurrence ? Arndt-Eistert Homologation ? Baeyer-Villiger Oxidation ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs 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 ? Hunsdiecker-Borodin Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Kinetics of Alkyl Halides ? Kumada Cross-Coupling Reaction ? Lawesson's Reagent ? Leuckart-Wallach 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 ? Preparation of Carboxylic Acids ? Prins Reaction ? 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 Dihalides ? Reformatsky Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Specialized Acylation Reagents-Ketenes ? 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
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