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[ CAS No. 57381-56-3 ] {[proInfo.proName]}

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Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 57381-56-3
Chemical Structure| 57381-56-3
Structure of 57381-56-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 57381-56-3 ]

CAS No. :57381-56-3 MDL No. :MFCD03094168
Formula : C7H3ClFN Boiling Point : -
Linear Structure Formula :- InChI Key :HBTXAKDVIXNVHZ-UHFFFAOYSA-N
M.W : 155.56 Pubchem ID :93656
Synonyms :

Calculated chemistry of [ 57381-56-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 36.12
TPSA : 23.79 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.76 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.77
Log Po/w (XLOGP3) : 2.09
Log Po/w (WLOGP) : 2.77
Log Po/w (MLOGP) : 2.48
Log Po/w (SILICOS-IT) : 2.86
Consensus Log Po/w : 2.39

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.57
Solubility : 0.423 mg/ml ; 0.00272 mol/l
Class : Soluble
Log S (Ali) : -2.22
Solubility : 0.938 mg/ml ; 0.00603 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.36
Solubility : 0.0673 mg/ml ; 0.000433 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.59

Safety of [ 57381-56-3 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P280-P305+P351+P338-P310 UN#:3439
Hazard Statements:H302-H311-H315-H319-H332 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 57381-56-3 ]

* 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 [ 57381-56-3 ]

[ 57381-56-3 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 463-71-8 ]
  • [ 16588-02-6 ]
  • [ 17417-09-3 ]
  • [ 39835-09-1 ]
  • [ 57381-56-3 ]
  • 5-Nitro-2-(trifluoromethylthio)benzonitrile [ No CAS ]
  • 2
  • [ 463-71-8 ]
  • [ 10199-89-0 ]
  • [ 17417-09-3 ]
  • [ 39835-09-1 ]
  • [ 57381-56-3 ]
  • 5-Nitro-2-(trifluoromethylthio)benzonitrile [ No CAS ]
  • 3
  • [ 109-01-3 ]
  • [ 57381-56-3 ]
  • [ 952282-00-7 ]
YieldReaction ConditionsOperation in experiment
66% Preparation 13: 1-[2-ChIoro-5-(4-methyI-piperazin-1-yl)-phenyl]-ethanone; STEP A; A mixture of <strong>[57381-56-3]2-chloro-5-fluoro-benzonitrile</strong> (1 g, 6.43 mmol), K2CO3 (2.66 g, 19.3 mmol) and 1-methyl-piperazine (1.02 g, 10.26 mmol) in DMSO (14 ml) was stirred at 1000C overnight and then further 1-methyl-piperazine (1.02 g, 10.26 mmol) was added. The mixture was stirred at 1000C overnight and then partitioned between water and Et2O. The organic phase was extracted with 1 M HCI and the aqueous layer was brought to basic conditions with NH4OH and extracted with DCM. The organic phase was dried over Na2SO4 and evaporated in vacuo to give 1 g of 2- chloro-5-(4-methyl-piperazin-1-yl)-benzonitrile. Y= 66%
  • 4
  • [ 57381-56-3 ]
  • [ 191171-55-8 ]
  • [ 1617497-63-8 ]
YieldReaction ConditionsOperation in experiment
77% With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In 1,4-dioxane; at 75 - 100℃; for 8.08333h;Inert atmosphere; General procedure: A solution of 2 M Na2CO3 (10 mL) was added under nitrogen to a 2-bromoaniline (10 mmol) in 60 mL dioxane. After 5 min stirring at 75 C, Pd[P(C6H5)3]4 was added followed by (10 mmol) of a 2-cyanophenylboronic acid pinacol ester. The reaction was stirred 8 h at 100 C. After cooling to rt the mixture was vacuum concentrated to half of its initial volume and extracted with CH2Cl2 (30 mL) and water (30 mL). The aqueous phase was extracted with CH2Cl2 (3×20 mL). The combined organic layers were washed with brine, dried over Na2SO4 and evaporated. The solid crystallized upon concentration.
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