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[ CAS No. 7298-67-1 ] {[proInfo.proName]}

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Chemical Structure| 7298-67-1
Chemical Structure| 7298-67-1
Structure of 7298-67-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 7298-67-1 ]

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Product Citations

Product Details of [ 7298-67-1 ]

CAS No. :7298-67-1 MDL No. :MFCD00100490
Formula : C10H11NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :DIQSYMRVTOVKQT-UHFFFAOYSA-N
M.W : 193.20 Pubchem ID :81720
Synonyms :

Calculated chemistry of [ 7298-67-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.2
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 52.97
TPSA : 66.4 ?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) : -6.78 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.3
Log Po/w (XLOGP3) : 0.98
Log Po/w (WLOGP) : 1.36
Log Po/w (MLOGP) : 0.6
Log Po/w (SILICOS-IT) : 1.28
Consensus Log Po/w : 1.1

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.77
Solubility : 3.25 mg/ml ; 0.0168 mol/l
Class : Very soluble
Log S (Ali) : -1.96
Solubility : 2.11 mg/ml ; 0.0109 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.55
Solubility : 0.546 mg/ml ; 0.00282 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.38

Safety of [ 7298-67-1 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 7298-67-1 ]

* 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 [ 7298-67-1 ]

[ 7298-67-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 7298-67-1 ]
  • [ 50-80-6 ]
YieldReaction ConditionsOperation in experiment
94% for 6 h; Heating / reflux 5-Acetamido-2-hydroxyacetophenone was hydrolyzed in 2N hydrochloric solution by refluxing for 6 hours, yielding 94percent of 5-amino-2-hydroxyacetophenone.
94% for 6 h; Heating / reflux 5. p-Anisidine is acylated at the amino center with acetic anhydride in di- chloromethane and the acylated product was obtained in 91 percent yield . Then, Friedel Craft's acylation was carried out to get the hydroxyacetophenone derivative with acetyl chloride in the presence of anhydrous aluminium chloride in DCM. The intermediate was isolated in 70percent yield. δ-Acetamido^-hydroxyacetophenone was hydrolyzed in 2N hydrochloric solution by refluxing for 6 h, yielding 94percent of δ-amino^-hydroxyacetophenone.
84% for 0.666667 h; Heating / reflux A suspension of [N- (3-ACETYL-4-HYDROXY-PHENYL)-] acetamide (1.029 g, 5.3 mmol) in [15percent] HC1 (1.5 ml, 6.2 mmol, 1.2 equ) was heated to reflux for 40 minutes, then cooled and neutralised with 10percent aqueous ammonia. The precipitated solid was collected by filtration as 1- (5-amino-2-hydroxy- phenyl) -ethanone (0.677 g, 84percent) a green solid. [APOS;H] nmr (400 MHz, CDC13) 2.58 (s, 3H) 3.47 (brs, 2H) 6.83 (d, [1H,] 8.8 Hz) 6.91 (dd, 1H, 2.8+8. 8 Hz) 7.02 (d, 1H, 2.8 Hz). 13C nmr (100 MHz, [CDC13)] 27.12 [(CH3)] 115.71 (CH) 119.40 (CH) 119.87 [(Q)] 125.737 (CH) 138.40 (Q) 156.03 (Q) 204.48 [(Q). EI+ 151.] 1 [(100percent, M+) C8HGNO2] Calc. 151.0633 Found 151.0632.
Reference: [1] Journal of Medicinal Chemistry, 1992, vol. 35, # 21, p. 3973 - 3976
[2] Patent: US2007/117823, 2007, A1, . Location in patent: Page/Page column 8
[3] Patent: WO2007/54580, 2007, A1, . Location in patent: Page/Page column 16
[4] European Journal of Medicinal Chemistry, 1991, vol. 26, # 9, p. 843 - 851
[5] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 9, p. 2079 - 2098
[6] Patent: WO2004/7475, 2004, A1, . Location in patent: Page 73-74
[7] Chemische Berichte, 1901, vol. 34, p. 125
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Technical Information

? Acidity of Phenols ? Acyl Group Substitution ? 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 ? Complex Metal Hydride Reductions ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Electrophilic Substitution of the Phenol Aromatic Ring ? Etherification Reaction of Phenolic Hydroxyl Group ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? Grignard Reaction ? Halogenation of Phenols ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? Mannich Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Oxidation of Phenols ? Passerini Reaction ? Paternò-Büchi Reaction ? Pechmann Coumarin Synthesis ? 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 Amines ? Reactions of Benzene and Substituted Benzenes ? Reformatsky Reaction ? Reimer-Tiemann Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Specialized Acylation Reagents-Carbodiimides and Related Reagents ? Specialized Acylation Reagents-Ketenes ? Specialized Acylation Reagents-Vilsmeier Reagent ? Stobbe Condensation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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