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[ CAS No. 211738-66-8 ] {[proInfo.proName]}

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Chemical Structure| 211738-66-8
Chemical Structure| 211738-66-8
Structure of 211738-66-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 211738-66-8 ]

CAS No. :211738-66-8 MDL No. :MFCD02253785
Formula : C6H7BrN2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :PFKHXPUGZRGBPX-UHFFFAOYSA-N
M.W : 219.04 Pubchem ID :605117
Synonyms :

Calculated chemistry of [ 211738-66-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.33
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 42.47
TPSA : 44.12 ?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) : -6.85 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.91
Log Po/w (XLOGP3) : 1.11
Log Po/w (WLOGP) : 0.97
Log Po/w (MLOGP) : 0.77
Log Po/w (SILICOS-IT) : 0.87
Consensus Log Po/w : 1.13

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.1
Solubility : 1.73 mg/ml ; 0.00791 mol/l
Class : Soluble
Log S (Ali) : -1.63
Solubility : 5.14 mg/ml ; 0.0235 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.73
Solubility : 4.05 mg/ml ; 0.0185 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.86

Safety of [ 211738-66-8 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 211738-66-8 ]

* 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 [ 211738-66-8 ]

[ 211738-66-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 637336-53-9 ]
  • [ 211738-66-8 ]
YieldReaction ConditionsOperation in experiment
35% With copper(I) bromide; copper(ll) bromide; isopentyl nitrite; In acetonitrile; at 80℃; for 2h; Isoamyl nitrite (1 .3 ml_, 9.67mmol) was added drop-wise to a suspension of methyl 4- amino-1 -methyl-1 H-pyrazole-3-carboxylate (p70, 1 g, 6.45 mmol), CuBr2 (1 .44 g, 6.45 mmol) and CuBr (924 mg, 6.45 mmol) in MeCN (25 ml_). The resulting mixture was stirred at 80 C for 2 hrs. After cooling to RT the volatiles were evaporated under vacuum and the residue was purified by FC on S1O2 column (eluting from cHex to 40% EtOAc) to afford methyl 4-bromo- 1 -methyl- 1 H-pyrazole-3-carboxylate (p71 , 500 mg, y= 35 %) as brown solid. MS (mlz): 220.9 [MH]+
500 mg With copper(I) bromide; copper(ll) bromide; isopentyl nitrite; In acetonitrile; at 80℃; for 2h; Isoamyl nitrite (1.3 ml_, 9.67mmol) was added drop-wise to a suspension of methyl 4- amino-1-methyl-1 H-pyrazole-3-carboxylate (p130, 1 g, 6.45 mmol), CuBr2 (1.44 g, 6.45 mmol) and CuBr (924 mg, 6.45 mmol) in MeCN (25 ml_). The resulting mixture was stirred at 80 C for 2 hrs. After cooling to RT the volatiles were evaporated under vacuum and the residue was purified by FC on S1O2 column (eluting from cHex to 40% EtOAc ) to afford methyl 4-bromo- 1 -methyl- 1 H-pyrazole-3-carboxylate (p131 , 500 mg, y= 35 %) as brown solid. MS (/77/z): 220.9 [MH]+
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