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[ CAS No. 25016-02-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 25016-02-8
Chemical Structure| 25016-02-8
Structure of 25016-02-8 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 25016-02-8 ]

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Product Details of [ 25016-02-8 ]

CAS No. :25016-02-8 MDL No. :MFCD02093683
Formula : C8H7NO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :YWVSKFXYEWMHEO-UHFFFAOYSA-N
M.W : 181.15 Pubchem ID :90685
Synonyms :

Calculated chemistry of [ 25016-02-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 47.14
TPSA : 72.12 ?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) : -6.15 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.23
Log Po/w (XLOGP3) : 1.77
Log Po/w (WLOGP) : 1.42
Log Po/w (MLOGP) : 0.03
Log Po/w (SILICOS-IT) : -0.17
Consensus Log Po/w : 0.85

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.22
Solubility : 1.09 mg/ml ; 0.006 mol/l
Class : Soluble
Log S (Ali) : -2.9
Solubility : 0.227 mg/ml ; 0.00125 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.85
Solubility : 2.54 mg/ml ; 0.014 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.65

Safety of [ 25016-02-8 ]

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 [ 25016-02-8 ]

* 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 [ 25016-02-8 ]

[ 25016-02-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 25016-02-8 ]
  • [ 5804-49-9 ]
YieldReaction ConditionsOperation in experiment
76% With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at -78 - 20℃; for 1h;Inert atmosphere; A solution of Intermediate 312B (410 mg, 2.263 mmol) in Toluene (11.500 mL) and THF (11.50 mL) was cooled to -78 C under an atmosphere of N2. DIBAL-H (1.0 Min Toluene) (3.40 mL, 3.40 mmol) was then added to the cooled solution dropwise. After the initial bubbling had subsided, the reaction mixture was allowed to thaw to room temperature. After 1 h, the reaction mixture was cooled to 0 C and quenched with 1.0 M HC1. The resulting suspension was stirred vigorously for 45 mm to fully cleave the aluminate complex. The mixture was then diluted with EtOAc and extracted. Theorganic phase was washed with brine, dried over MgSO4, filtered and concentrated. The resulting crude product was purified by ISCO (80g, 0-100% EtOAc/Hexanes, 33 mm. Product at 50%) to give Intermediate 312C (370 mg, 1.717 mmol, 76% yield) as a light yellow solid. LC-MS. Method H, RT = 0.68 mm, MS (ESI) m/z: 184.0 (M+H). ?H NMR (4001V11{z, CHLOROFORM-d) 8.29 (d, J=2.9 Hz, 1H), 8.21 (dd, J9.0, 2.6 Hz,1H), 6.94 (d, J=9.0 Hz, 1H), 4.75 (d, J=6.4 Hz, 2H), 3.97 (s, 3H), 2.07 (t, J=6.4 Hz, 1H).
  • 2
  • [ 25016-02-8 ]
  • [ 3913-23-3 ]
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Technical Information

? Acidity of Phenols ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Chan-Lam Coupling Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Chaykovsky Reaction ? Corey-Fuchs 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 ? Hantzsch Dihydropyridine Synthesis ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Julia-Kocienski Olefination ? Knoevenagel Condensation ? Leuckart-Wallach Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mukaiyama Aldol Reaction ? Nomenclature of Ethers ? Nozaki-Hiyama-Kishi Reaction ? Oxidation of Phenols ? Passerini Reaction ? Paternò-Büchi Reaction ? Pechmann Coumarin Synthesis ? Petasis Reaction ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Preparation of Ethers ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions of Ethers ? Reformatsky Reaction ? Reimer-Tiemann Reaction ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Stetter Reaction ? Stobbe Condensation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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