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[ CAS No. 20358-07-0 ] {[proInfo.proName]}

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Chemical Structure| 20358-07-0
Chemical Structure| 20358-07-0
Structure of 20358-07-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 20358-07-0 ]

CAS No. :20358-07-0 MDL No. :MFCD05664560
Formula : C7H5FN2S Boiling Point : -
Linear Structure Formula :- InChI Key :YHBIGBYIUMCLJS-UHFFFAOYSA-N
M.W : 168.19 Pubchem ID :821203
Synonyms :

Calculated chemistry of [ 20358-07-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.98
TPSA : 67.15 ?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) : -5.81 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.67
Log Po/w (XLOGP3) : 2.13
Log Po/w (WLOGP) : 2.45
Log Po/w (MLOGP) : 1.69
Log Po/w (SILICOS-IT) : 2.85
Consensus Log Po/w : 2.16

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.83
Solubility : 0.249 mg/ml ; 0.00148 mol/l
Class : Soluble
Log S (Ali) : -3.17
Solubility : 0.113 mg/ml ; 0.000674 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.88
Solubility : 0.22 mg/ml ; 0.00131 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.06

Safety of [ 20358-07-0 ]

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

Application In Synthesis of [ 20358-07-0 ]

* 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 [ 20358-07-0 ]

[ 20358-07-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 20358-07-0 ]
  • [ 154327-27-2 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; copper; sodium nitrite; In water; STR159 A solution of 242 g (3.5 mol) of sodium nitrite in 440 ml of water is added dropwise with stirring to a mixture, cooled to -10° C., of 147 g (0.87 mol) of 2-amino-5-fluoro-benzothiazole, 1700 ml of conc. hydrochloric acid and 20 g of copper power and the reaction mixture is stirred at 0° C. for 60 minutes and at 50° C. for a further 60 minutes. It is then extracted with chloroform and the solvent is carefully removed by distillation from the organic phase in a water-jet vacuum. 80 g (49percent of theory) of 2-chloro-5-fluoro-benzothiazole are obtained as a crystalline residue of melting point 69° C.
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