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[ CAS No. 98612-60-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 98612-60-3
Chemical Structure| 98612-60-3
Structure of 98612-60-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 98612-60-3 ]

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Product Citations

Product Details of [ 98612-60-3 ]

CAS No. :98612-60-3 MDL No. :MFCD06799465
Formula : C5H8BrNO Boiling Point : No data available
Linear Structure Formula :- InChI Key :QFOSFXPTXNRRMF-SCSAIBSYSA-N
M.W : 178.03 Pubchem ID :12593790
Synonyms :

Calculated chemistry of [ 98612-60-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.8
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 38.82
TPSA : 29.1 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.18 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.47
Log Po/w (XLOGP3) : 0.29
Log Po/w (WLOGP) : 0.28
Log Po/w (MLOGP) : 0.65
Log Po/w (SILICOS-IT) : 1.52
Consensus Log Po/w : 0.84

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.06
Solubility : 15.5 mg/ml ; 0.087 mol/l
Class : Very soluble
Log S (Ali) : -0.46
Solubility : 61.3 mg/ml ; 0.344 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.95
Solubility : 1.98 mg/ml ; 0.0111 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.41

Safety of [ 98612-60-3 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H302-H317-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 98612-60-3 ]

* 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.

  • Upstream synthesis route of [ 98612-60-3 ]
  • Downstream synthetic route of [ 98612-60-3 ]

[ 98612-60-3 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 128899-31-0 ]
  • [ 98612-60-3 ]
YieldReaction ConditionsOperation in experiment
90% With lithium bromide In acetone at 80℃; To a solution of (R)-(5-oxopyrrolidin-2-yl)methyl 4-methylbenzenesulfonate (5.0 g, 18.5 mmol) in acetone (10 mL) was added lithium bromide (4.8 g, 55.6 mmol) and the reaction mixture stirred at 80 00 overnight. The solvent was then removed in vacuo and the reaction mixture partitioned between H20 (50 mL) and EtOAc (100 mL). The aqueous layer was extracted with EtOAc (2 x 100 mL), combined organics dried(Na2504), the solvent removed in vacuo and the residue purified by column chromatography (normal basic activated alumina, at 0.2 to 1.0 percent MeOH in DOM) to give (R)-5-(bromomethyl)pyrrolidin-2-one (3.0 g, 90 percent) as a light yellow liquid.LCMS (Method F): m/z 178/180 (M+H) (ES), at 2.24 mm, UV active
Reference: [1] Patent: WO2017/21728, 2017, A1, . Location in patent: Page/Page column 45; 46
  • 2
  • [ 66673-40-3 ]
  • [ 98612-60-3 ]
Reference: [1] Helvetica Chimica Acta, 1990, vol. 73, # 1, p. 122 - 132
[2] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 18, p. 4043 - 4047
[3] Patent: WO2012/154777, 2012, A1, . Location in patent: Page/Page column 125-126
[4] Patent: WO2014/65791, 2014, A1, . Location in patent: Page/Page column 142; 143
[5] Patent: WO2017/21728, 2017, A1,
[6] Organic Letters, 2019, vol. 21, # 3, p. 793 - 796
  • 3
  • [ 6893-26-1 ]
  • [ 98612-60-3 ]
Reference: [1] Helvetica Chimica Acta, 1990, vol. 73, # 1, p. 122 - 132
  • 4
  • [ 64700-65-8 ]
  • [ 98612-60-3 ]
Reference: [1] Helvetica Chimica Acta, 1990, vol. 73, # 1, p. 122 - 132
  • 5
  • [ 4042-36-8 ]
  • [ 98612-60-3 ]
Reference: [1] Helvetica Chimica Acta, 1990, vol. 73, # 1, p. 122 - 132
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