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[ CAS No. 6656-49-1 ] {[proInfo.proName]}

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Type HazMat fee for 500 gram (Estimated)
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Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 6656-49-1
Chemical Structure| 6656-49-1
Structure of 6656-49-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 6656-49-1 ]

CAS No. :6656-49-1 MDL No. :MFCD00042322
Formula : C8H6F3NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :KQUQBPVYIURTNZ-UHFFFAOYSA-N
M.W : 205.13 Pubchem ID :81171
Synonyms :

Calculated chemistry of [ 6656-49-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 2
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 45.23
TPSA : 45.82 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.17 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.79
Log Po/w (XLOGP3) : 3.35
Log Po/w (WLOGP) : 4.07
Log Po/w (MLOGP) : 2.27
Log Po/w (SILICOS-IT) : 1.17
Consensus Log Po/w : 2.53

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.41
Solubility : 0.0803 mg/ml ; 0.000391 mol/l
Class : Soluble
Log S (Ali) : -3.99
Solubility : 0.021 mg/ml ; 0.000102 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.06
Solubility : 0.179 mg/ml ; 0.000875 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.87

Safety of [ 6656-49-1 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P280-P305+P351+P338-P311 UN#:2810
Hazard Statements:H301+H311+H331-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 6656-49-1 ]

* 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 [ 6656-49-1 ]

[ 6656-49-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 6656-49-1 ]
  • [ 54396-44-0 ]
YieldReaction ConditionsOperation in experiment
92% With hydrogen; In methanol; C. 3-Amino-2-Methylbenzotrifluoride A solution of 2-methyl-3-nitrobenzotrifluoride (41.0 g, 0.2 m) in methanol (100 ml) was stirred under an atmosphere of dry nitrogen at room temperature and palladium on charcoal catalyst (10percent w/w, 1.0 g) was added. The stirred mixture was warmed to 40°-45° and then hydrogen was passed into the solution at atmospheric pressure until the reduction, as observed by thin-layer chromatography, was complete (4-5 hours). The solution was cooled to room temperature and the catalyst removed by filtration. Distillation of the solvent at atmospheric pressure followed by steam distillation of the crude product gave 3-amino-2-methylbenzotrifluoride (32.2 g, 92percent yield), as a pale-brown oil which slowly crystallized.
palladium; 187 g. of 2-nitro-6-trifluoromethyltoluene were reduced with hydrogen over a palladium-on-carbon catalyst to yield 153.9 g. of a red oil comprising 3-trifluoromethyl-2-methylaniline.
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