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[ CAS No. 101-79-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 101-79-1
Chemical Structure| 101-79-1
Structure of 101-79-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 101-79-1 ]

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Product Details of [ 101-79-1 ]

CAS No. :101-79-1 MDL No. :MFCD00043925
Formula : C12H10ClNO Boiling Point : -
Linear Structure Formula :- InChI Key :YTISFYMPVILQRL-UHFFFAOYSA-N
M.W : 219.67 Pubchem ID :7578
Synonyms :

Calculated chemistry of [ 101-79-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 62.37
TPSA : 35.25 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.74 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.45
Log Po/w (XLOGP3) : 2.67
Log Po/w (WLOGP) : 3.72
Log Po/w (MLOGP) : 3.22
Log Po/w (SILICOS-IT) : 2.94
Consensus Log Po/w : 3.0

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.34
Solubility : 0.0995 mg/ml ; 0.000453 mol/l
Class : Soluble
Log S (Ali) : -3.06
Solubility : 0.19 mg/ml ; 0.000867 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.92
Solubility : 0.00265 mg/ml ; 0.0000121 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 1.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.64

Safety of [ 101-79-1 ]

Signal Word:Danger Class:9
Precautionary Statements:P261-P264-P270-P272-P273-P280-P301+P312+P330-P302+P352-P305+P351+P338+P310-P333+P313-P391-P501 UN#:3077
Hazard Statements:H302-H317-H318-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 101-79-1 ]

* 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.

  • Downstream synthetic route of [ 101-79-1 ]

[ 101-79-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 33332-28-4 ]
  • [ 101-79-1 ]
  • [ 1366234-22-1 ]
  • 2
  • [ 61929-24-6 ]
  • [ 101-79-1 ]
  • [ 1562690-58-7 ]
YieldReaction ConditionsOperation in experiment
28% With toluene-4-sulfonic acid; In isopropyl alcohol; at 60 - 80℃;Inert atmosphere; [0197] To a solution of Compound 7-A (1.35 g, 6.2 mmol) and compound 7-B (0.4 g,mmol) in isopropanol (25 mL) was added p-toluenesulfonic acid (1.16 g, 6.1 mmol). The resulting mixture was stirred overnight at about 60-80 C overnight under nitrogen. Monitoring by thin layer chromatography (petrol ether: ethyl acetate=2: 1 and Rf at 0.5) showed the reaction was complete. The mixture was diluted with saturated aqueous NaHCO3 (90 mL) and extracted with ethyl acetate (30 mL x 3). The organic layers were concentrated and purified by silica gel column (petrol ether: ethyl acetate= 15:1) to give the title compound (206 mg, 28%) as a solid. ?H NMR (400 MHz, DMSO) oe 6.97-6.95 (d, J=Hz, 1H), 7.06-7.04 (d, J= 8.4 Hz, 1H), 7.39-7.37 (d, J= 8.4 Hz, 1H), 7.67-7.65 (d, J=Hz, 1H), 8.87 (s, 1H), 10.39 (s, 1H). MS: 303.9 (M+lj.
  • 3
  • [ 53911-68-5 ]
  • [ 101-79-1 ]
  • 5-((4-(4-chlorophenoxy)phenyl)amino)-3-(4-chlorophenyl)-5-oxopentanoic acid [ No CAS ]
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