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[ CAS No. 50413-30-4 ] {[proInfo.proName]}

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Chemical Structure| 50413-30-4
Chemical Structure| 50413-30-4
Structure of 50413-30-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 50413-30-4 ]

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Product Details of [ 50413-30-4 ]

CAS No. :50413-30-4 MDL No. :MFCD06658470
Formula : C9H11NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :CEKCJQBZVNIMLD-UHFFFAOYSA-N
M.W : 181.19 Pubchem ID :12919999
Synonyms :

Calculated chemistry of [ 50413-30-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 48.62
TPSA : 61.55 ?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) : -5.53 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.72
Log Po/w (XLOGP3) : 2.64
Log Po/w (WLOGP) : 1.07
Log Po/w (MLOGP) : 1.06
Log Po/w (SILICOS-IT) : 0.99
Consensus Log Po/w : 1.5

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.77
Solubility : 0.308 mg/ml ; 0.0017 mol/l
Class : Soluble
Log S (Ali) : -3.58
Solubility : 0.0473 mg/ml ; 0.000261 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.24
Solubility : 1.04 mg/ml ; 0.00573 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.41

Safety of [ 50413-30-4 ]

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

Application In Synthesis of [ 50413-30-4 ]

* 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 [ 50413-30-4 ]

[ 50413-30-4 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 108-30-5 ]
  • [ 50413-30-4 ]
  • [ 108489-18-5 ]
  • 2
  • [ 50413-30-4 ]
  • [ 144-62-7 ]
  • 2-hydroxyoxalylamino-4-methoxy-benzoic acid methyl ester [ No CAS ]
  • 3
  • [ 50413-30-4 ]
  • [ 77287-34-4 ]
  • [ 16064-24-7 ]
  • 5
  • [ 67-56-1 ]
  • 2-Amino-4-methoxy-benzoyl chloride [ No CAS ]
  • [ 50413-30-4 ]
  • 6
  • [ 50413-30-4 ]
  • [ 98-59-9 ]
  • [ 93009-62-2 ]
YieldReaction ConditionsOperation in experiment
70% With pyridine; at 20℃; for 16h; To a stirred solution of compound If-I (7 g, 38.6 mmol) in pyridine (80 ml) was slowly added TsCI (8.8 g, 46.6 mmol) at rt. This solution was further stirred for 16h. The reaction mixture was poured into cold water upon which a solid was formed. The precipitate was filtered off and washed with n-pentane (50 ml) to afford the title compound If-2 as an off-white solid (10.8 g, 70% yield). LCMS [M+H] 336.
  • 7
  • [ 67-56-1 ]
  • [ 4294-95-5 ]
  • [ 50413-30-4 ]
YieldReaction ConditionsOperation in experiment
75.92% With sulfuric acid; for 24h;Reflux; To a solution of 2-amino-4-methoxybenzoic acid 33 (5.0 g,0.03 mol) in methanol (50 mL) was added strong sulphuricacid (9 mL). The solution was stirred at reflux for 24 h. Itwas cooled to room temperature and the pH of the mixturewas adjusted to 5~6 with saturated sodium carbonatesolution. The solution was extracted with EA (100 mL*2).The combined organic layers were washed with brine(50 mL), dried over Na2SO4, filtered and concentrated,affording white powder 34 (4.11 g, 75.92%). 34: 1H NMR (400 MHz, CDCl3) 7.81 (d, J = 8.9 Hz, 1 H), 6.25 (dd, J =9.0, 2.5 Hz, 1H), 6.13 (d, J = 2.4 Hz, 1H), 5.80 (s, 2H), 3.86(s, 3H), 3.81 (s, 3H).
37% With sulfuric acid;Reflux; Step a): Methyl 2-amino-4-methoxybenzoate 1000 mg (6.0 mmol) of 2-amino-4-methoxybenzoic acid are reacted according to General Method I. Yield: 400 mg (37% of theory) LC-MS (Method 3): Rt=1.96 min; MS (ESIpos): m/z=182 [M+H]+. 5 mmol of the carboxylic acid are dissolved in 50 ml of methanol, and 5 ml of concentrated sulfuric acid are added. The mixture is heated under reflux for 14-24 h. After cooling to room temperature, the solution is poured onto ice and adjusted to pH 6 using sodium bicarbonate. After addition of 100 ml of dichloromethane, the aqueous phase is separated off and reextracted twice with in each case 50 ml of dichloromethane. The combined organic extracts are dried over sodium sulfate, filtered and concentrated under reduced pressure.
  • 8
  • [ 67-56-1 ]
  • 2-amino-4-methoxy-benzoic acid-hydrochloride [ No CAS ]
  • [ 50413-30-4 ]
  • 9
  • [ 50413-30-4 ]
  • [ 4637-24-5 ]
  • 2-(dimethylamino-methyleneamino)-4-methoxy-benzoic acid methyl ester [ No CAS ]
  • 12
  • [ 50413-30-4 ]
  • 7-hydroxy-4-oxo-1,4-dihydro-quinoline-3-carbonitrile [ No CAS ]
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