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[ CAS No. 2832-19-1 ] {[proInfo.proName]}

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Chemical Structure| 2832-19-1
Chemical Structure| 2832-19-1
Structure of 2832-19-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2832-19-1 ]

CAS No. :2832-19-1 MDL No. :MFCD00021961
Formula : C3H6ClNO2 Boiling Point : -
Linear Structure Formula :ClCH2CONHCH2OH InChI Key :TXNSZCSYBXHETP-UHFFFAOYSA-N
M.W : 123.54 Pubchem ID :62466
Synonyms :

Calculated chemistry of [ 2832-19-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.67
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 25.49
TPSA : 49.33 ?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) : -7.35 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.26
Log Po/w (XLOGP3) : -0.42
Log Po/w (WLOGP) : -0.71
Log Po/w (MLOGP) : -0.39
Log Po/w (SILICOS-IT) : -0.1
Consensus Log Po/w : -0.07

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.14
Solubility : 88.8 mg/ml ; 0.719 mol/l
Class : Very soluble
Log S (Ali) : -0.15
Solubility : 87.2 mg/ml ; 0.706 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.69
Solubility : 25.5 mg/ml ; 0.206 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.52

Safety of [ 2832-19-1 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3261
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2832-19-1 ]

* 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 [ 2832-19-1 ]

[ 2832-19-1 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 2832-19-1 ]
  • [ 827-99-6 ]
  • [ 562080-94-8 ]
YieldReaction ConditionsOperation in experiment
33.8% In concentrated sulfuric acid; acetic acid; EXAMPLE 73 2-Chloro-N-(2-hydroxy-4-trifluoromethoxy-benzyl)-acetamide <strong>[827-99-6]3-(Trifluoromethoxy)phenol</strong> (4.827 g, 27 mmol) was dissolved in glacial acetic acid (20 mL). The mixture was cooled in an ice bath between 14-17° C. and concentrated sulfuric acid (2 mL) was slowly added keeping the temperature below 20° C. The mixture was cooled below 10° C. and N-hydroxymethyl-2-chloroacetamide (3.52 g, 28.5 mmol) was added. The mixture was warmed slowly to room temperature and stirred overnight. The mixture was then poured slowly into ice (200 mL) and the pH was adjusted to ~4-5 with KOH pellets, keeping the temperature below 5° C. The reaction mixture was warmed to room temperature and extracted twice with ethyl acetate (150 mL). The organic layer was collected and washed with NaHCO3 (sat., 30 mL). The organic layer was dried over MgSO4, filtered and the solvent removed to dryness. The mixture was purified by column chromatography (SiO2, 700 mL) using an eluent of hexane/ethyl acetate (10/2). Recovery: 2.42 g (33.8percent yield). 1H NMR (DMSO) delta=10.23 (1H, s), 8.56 (1H, st), 7.16-7.14 (1H, sd), 6.71-6.70 (2H, br), 4.18-4.17 (2H, d), 4.08 (2H, s).
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