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[ CAS No. 267225-27-4 ] {[proInfo.proName]}

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Chemical Structure| 267225-27-4
Chemical Structure| 267225-27-4
Structure of 267225-27-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 267225-27-4 ]

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Product Details of [ 267225-27-4 ]

CAS No. :267225-27-4 MDL No. :MFCD03092959
Formula : C9H10BrNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :JFVLNTLXEZDFHW-MRVPVSSYSA-N
M.W : 244.09 Pubchem ID :7023575
Synonyms :

Calculated chemistry of [ 267225-27-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 53.2
TPSA : 63.32 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -8.3 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.35
Log Po/w (XLOGP3) : -0.72
Log Po/w (WLOGP) : 1.4
Log Po/w (MLOGP) : -0.39
Log Po/w (SILICOS-IT) : 1.55
Consensus Log Po/w : 0.64

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.04
Solubility : 22.1 mg/ml ; 0.0905 mol/l
Class : Very soluble
Log S (Ali) : -0.13
Solubility : 179.0 mg/ml ; 0.735 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.72
Solubility : 0.461 mg/ml ; 0.00189 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.13

Safety of [ 267225-27-4 ]

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 [ 267225-27-4 ]

* 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 [ 267225-27-4 ]

[ 267225-27-4 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 7345-79-1 ]
  • [ 267225-27-4 ]
  • [ 42538-40-9 ]
  • (S)-3-amino-3-(2-bromophenyl)propionic acid [ No CAS ]
  • 2
  • [ 7345-79-1 ]
  • [ 267225-27-4 ]
  • [ 42538-40-9 ]
  • 3
  • [ 120240-65-5 ]
  • [ 3060-50-2 ]
  • [ 119-61-9 ]
  • [ 267225-27-4 ]
  • [ 42538-40-9 ]
YieldReaction ConditionsOperation in experiment
With C39H33N3O2*2ClH; In methanol; water; at 20℃; for 72h; General procedure: To a 5 mL vial equipped with a magnetic stirrer bar were added 3-cyclohexyl-2-oxopropanoic acid (1j) (0.0510 g, 0.30 mmol), 2,2-diphenylglycine (2) (0.0681 g, 0.30 mmol), chiral pyridoxamine 6g (0.0195 g, 0.030 mmol), and MeOH-H2O (8:2) (3.0 mL). The mixture was stirred at 20 °C for 3 days. The reaction mixture was transferred to a 25 mL round-bottom flask and MeOH was added until all the solid was dissolved. Then silica gel (0.50 g) was added. After removal of the solvent in vacuo at 20 °C, the resulting residue was submitted to column chromatography on silica gel (EtOH/ethyl acetate/25-28percent ammonia solution =100:58:16) to give compound 3j (0.0401 g, 78percent yield, 52percent ee) as a white solid. The enantiomeric excesses of 3b-k were deteremined by HPLC analysis after being converted to N-benzoyl methyl esters by treatment with thionyl chloride in methanol and subsequent reaction benzoyl chloride.7 The enantiomeric excess of 3a was deteremined by HPLC analysis after being converted to its methyl ester by treatment with CH2N2 in methanol.
YieldReaction ConditionsOperation in experiment
With C39H33N3O2*2ClH; water; 2,2-diphenylglycine; In methanol; at 20℃; for 72h; General procedure: Take 5mL of the reaction bottle. Was weighed into the flask the keto acid 2a (0.046 g, 0.20 mmol), the chiral pyridoxamine catalyst 1a (0.013 g, 0.020 mmol), and 2,2-diphenylglycine 14 (0.045 g, 0.20 mmol). To the flask was added MeOH (1.6 mL) and water (0.4 mL). Adding a magnet, plug a good stopper, placed in 20°C constant temperature reaction tank reaction for 3d. The reaction was stopped. The contents of the flask were transferred to a 25 mL eggplant flask. 10 mL of methanol was added to dissolve all the solids in the flask. Silica gel (0.2 g) was added. The solvent was removed at room temperature. Dry on the column. Silica gel column chromatography gave the product amino acid 3a (0.023 g, 50percent). The ee value of 3a was obtained by HPLC analysis of its carboxymethylated derivative with an ee value of 34percent.
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