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[ CAS No. 114772-38-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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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+
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Chemical Structure| 114772-38-2
Chemical Structure| 114772-38-2
Structure of 114772-38-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 114772-38-2 ]

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Product Details of [ 114772-38-2 ]

CAS No. :114772-38-2 MDL No. :MFCD06200816
Formula : C15H13BrO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :RMXGTMRDXKUUDJ-UHFFFAOYSA-N
M.W : 305.17 Pubchem ID :11012181
Synonyms :

Calculated chemistry of [ 114772-38-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.13
Num. rotatable bonds : 4
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 75.99
TPSA : 26.3 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.92 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.97
Log Po/w (XLOGP3) : 4.57
Log Po/w (WLOGP) : 3.88
Log Po/w (MLOGP) : 4.04
Log Po/w (SILICOS-IT) : 4.45
Consensus Log Po/w : 3.98

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.84
Solubility : 0.00441 mg/ml ; 0.0000144 mol/l
Class : Moderately soluble
Log S (Ali) : -4.85
Solubility : 0.00435 mg/ml ; 0.0000143 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -6.23
Solubility : 0.000178 mg/ml ; 0.000000583 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.3

Safety of [ 114772-38-2 ]

Signal Word:Danger Class:8
Precautionary Statements:P501-P260-P234-P264-P280-P390-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P406-P405 UN#:3261
Hazard Statements:H314-H290 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 114772-38-2 ]

* 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 [ 114772-38-2 ]

[ 114772-38-2 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 50790-93-7 ]
  • [ 114772-38-2 ]
  • 4'-(2-Butyl-imidazol-1-ylmethyl)-biphenyl-2-carboxylic acid methyl ester [ No CAS ]
  • 2
  • [ 57113-90-3 ]
  • [ 114772-38-2 ]
  • [ 150058-11-0 ]
  • 3
  • [ 1019-85-8 ]
  • [ 114772-38-2 ]
  • methyl 4'-[(2-p-chlorophenyl-1H-benzimidazol-1-yl)methyl]biphenyl-2-carboxylate [ No CAS ]
  • 4
  • [ 114772-38-2 ]
  • [ 152628-03-0 ]
  • [ 884330-11-4 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide; In N,N-dimethyl acetamide; at 80 - 85℃; for 2 - 3h; EXAMPLE 17; PREPARATION OF METHYL 4.-[2-n-PROPYL-4- METHYL-6-CARBOXYLIC ACID-BENZIMIDAZOL-1-YL] -METHYL-BIPHENYL-2-CARBOXYLATE (FORMULA XIV); 10 g of 2-n-propyl-4-methyl-benzimidazole-6-carboxylic acid of Example 1 , 19.8 g of 4'-(bromomethyl)biphenyl-2-carboxylate, and 6.4 g of potassium hydroxide were charged into a round bottom flask containing 100 ml of N,N- dimethyl acetamide. The contents were heated to 80-85 C and stirred for 2-3 hours. Reaction completion was confirmed by thin layer chromatography and the mass was cooled to 25-35 C. Charged 100 ml of water and extracted the product with ethyl acetate (3 x 450 ml). Organic layer was washed with water (2 x 100 ml) and then the solvent was distilled completely under vacuum. 100 ml of acetone was charged to the residue at room temperature and stirred for 30-45 minutes. Filtered the solid and washed with acetone (20 ml). Dried the solid at 50-55 C for 4-5 hours to get 21 g of the title compound.
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