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[ CAS No. 2646-90-4 ] {[proInfo.proName]}

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Chemical Structure| 2646-90-4
Chemical Structure| 2646-90-4
Structure of 2646-90-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2646-90-4 ]

CAS No. :2646-90-4 MDL No. :MFCD00010327
Formula : C7H4F2O Boiling Point : No data available
Linear Structure Formula :- InChI Key :VVVOJODFBWBNBI-UHFFFAOYSA-N
M.W : 142.10 Pubchem ID :137663
Synonyms :

Calculated chemistry of [ 2646-90-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 31.75
TPSA : 17.07 ?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) : -5.83 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.54
Log Po/w (XLOGP3) : 1.88
Log Po/w (WLOGP) : 2.62
Log Po/w (MLOGP) : 2.32
Log Po/w (SILICOS-IT) : 2.82
Consensus Log Po/w : 2.24

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.28
Solubility : 0.74 mg/ml ; 0.00521 mol/l
Class : Soluble
Log S (Ali) : -1.86
Solubility : 1.96 mg/ml ; 0.0138 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.88
Solubility : 0.188 mg/ml ; 0.00132 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.01

Safety of [ 2646-90-4 ]

Signal Word:Danger Class:3
Precautionary Statements:P261-P305+P351+P338 UN#:1989
Hazard Statements:H225-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2646-90-4 ]

* 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 [ 2646-90-4 ]

[ 2646-90-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 20173-04-0 ]
  • [ 21512-16-3 ]
  • [ 2646-90-4 ]
  • [ 1437787-00-2 ]
  • 2
  • [ 2646-90-4 ]
  • [ 1218935-59-1 ]
  • 3
  • [ 2646-90-4 ]
  • [ 405939-39-1 ]
  • tert-butyl (5-((2,5-difluorophenyl)(hydroxy)methyl)thiazol-2-yl)carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
24% Dissolved ferf-butyl (5-bromothiazol-2-yl)carbamate (0.5 g, 1 .79 mmol) in tetrahydrofuran (8.95 ml_ ) and cooled to -78 C. Carefully added n-butyllithium (1 .6M in hexanes, 1 .14 ml_, 2.86 mmol) and stirred for 10 minutes, followed by 2,5-difluorobenzaldehyde (271 uL, 2.50 mmol). Stirred at -78 C for 3 h. Warmed to room temperature and quenched with saturated aqueous ammonium chloride (15 ml_). Extracted with ethyl acetate (20 ml_) and washed with brine (15 ml_). The combined organic layers were dried over sodium sulfate, filtered, and concentrated. Purified reaction by column chromatography (eluting with 0-50% ethyl acetate/hexanes through 24 g of silica gel) to give ferf-butyl (5-((2,5-difluorophenyl)(hydroxy)methyl)thiazol-2-yl)carbamate as a yellow solid (150 mg, 0.438 mmol, 24%). 1 H NMR (300 MHz, Chloroform-d) d 7.37 (d, J = 3.0 Hz, 1 H), 7.17 (s, 1 H), 7.10 - 6.92 (m, 2H), 6.27 (s, 1 H), 1 .53 (s, 9H).
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