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[ CAS No. 103003-01-6 ] {[proInfo.proName]}

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Chemical Structure| 103003-01-6
Chemical Structure| 103003-01-6
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Product Details of [ 103003-01-6 ]

CAS No. :103003-01-6 MDL No. :MFCD03426271
Formula : C5H11NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :VLAZLCVSFAYIIL-UHFFFAOYSA-N
M.W : 117.15 Pubchem ID :3497988
Synonyms :

Calculated chemistry of [ 103003-01-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 33.0
TPSA : 41.49 ?2

Pharmacokinetics

GI absorption : Low
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) : -7.87 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.45
Log Po/w (XLOGP3) : -1.2
Log Po/w (WLOGP) : -1.41
Log Po/w (MLOGP) : -1.04
Log Po/w (SILICOS-IT) : 0.43
Consensus Log Po/w : -0.36

Druglikeness

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

Water Solubility

Log S (ESOL) : 0.26
Solubility : 211.0 mg/ml ; 1.8 mol/l
Class : Highly soluble
Log S (Ali) : 0.82
Solubility : 779.0 mg/ml ; 6.65 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.33
Solubility : 55.2 mg/ml ; 0.471 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.12

Safety of [ 103003-01-6 ]

Signal Word:Warning Class:
Precautionary Statements:P301+P312+P330 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 103003-01-6 ]

* 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 [ 103003-01-6 ]
  • Downstream synthetic route of [ 103003-01-6 ]

[ 103003-01-6 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 189321-66-2 ]
  • [ 103003-01-6 ]
YieldReaction ConditionsOperation in experiment
26% With borane In tetrahydrofuran at 0 - 20℃; for 2.5 h; To N-Boc morpholine-2-carboxylic acid (2g) in THF (5ML) at 0°C was added a solution of borane. THF complex (1 N, 10. 38MOI) and the mixture was stirred for 30min at 0°C, and for 2hr at room temperature. Water (200ml) was added to the reaction and the mixture extracted with CH2CI2, dried with NA2SO4, and concentrated in vacuo to give 490mg of product (26percent). The product was then stirred in 4N HCI/DIOXANE to give the amine salt.
Reference: [1] Patent: WO2004/33440, 2004, A1, . Location in patent: Page 173
  • 2
  • [ 40987-24-4 ]
  • [ 103003-01-6 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 1985, vol. 33, # 9, p. 3766 - 3774
[2] Journal of Medicinal Chemistry, 1994, vol. 37, # 17, p. 2791 - 2796
[3] Journal of Medicinal Chemistry, 2017, vol. 60, # 6, p. 2227 - 2244
  • 3
  • [ 1542717-38-3 ]
  • [ 103003-01-6 ]
Reference: [1] Journal of Organic Chemistry, 2014, vol. 79, # 10, p. 4644 - 4649
  • 4
  • [ 885953-31-1 ]
  • [ 103003-01-6 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 18, p. 5440 - 5443
  • 5
  • [ 1607004-67-0 ]
  • [ 103003-01-6 ]
Reference: [1] Journal of Organic Chemistry, 2014, vol. 79, # 10, p. 4644 - 4649
  • 6
  • [ 1607004-58-9 ]
  • [ 103003-01-6 ]
Reference: [1] Journal of Organic Chemistry, 2014, vol. 79, # 10, p. 4644 - 4649
  • 7
  • [ 1607004-68-1 ]
  • [ 103003-01-6 ]
Reference: [1] Journal of Organic Chemistry, 2014, vol. 79, # 10, p. 4644 - 4649
  • 8
  • [ 40987-25-5 ]
  • [ 103003-01-6 ]
Reference: [1] Journal of Medicinal Chemistry, 2017, vol. 60, # 6, p. 2227 - 2244
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