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[ CAS No. 625-05-8 ] {[proInfo.proName]}

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Chemical Structure| 625-05-8
Chemical Structure| 625-05-8
Structure of 625-05-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 625-05-8 ]

CAS No. :625-05-8 MDL No. :MFCD06245495
Formula : C5H11NO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :NFQAIWOMJQWGSS-UHFFFAOYSA-N
M.W : 117.15 Pubchem ID :2760933
Synonyms :

Calculated chemistry of [ 625-05-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.8
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 30.67
TPSA : 63.32 Ų

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) : -9.06 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.88
Log Po/w (XLOGP3) : -2.88
Log Po/w (WLOGP) : 0.2
Log Po/w (MLOGP) : 0.01
Log Po/w (SILICOS-IT) : -0.53
Consensus Log Po/w : -0.46

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : 1.38
Solubility : 2810.0 mg/ml ; 24.0 mol/l
Class : Highly soluble
Log S (Ali) : 2.11
Solubility : 15000.0 mg/ml ; 128.0 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.07
Solubility : 99.7 mg/ml ; 0.851 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 625-05-8 ]

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 [ 625-05-8 ]

* 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 [ 625-05-8 ]

[ 625-05-8 ] Synthesis Path-Downstream   1~22

  • 2
  • [ 19805-83-5 ]
  • [ 625-05-8 ]
  • 3
  • [ 625-05-8 ]
  • [ 98-88-4 ]
  • [ 17207-42-0 ]
  • 4
  • [ 625-05-8 ]
  • [ 79-04-9 ]
  • [ 501095-35-8 ]
  • 5
  • [ 75-77-4 ]
  • [ 625-05-8 ]
  • [ 58521-59-8 ]
  • 7
  • [ 625-05-8 ]
  • [ 18931-20-9 ]
  • [ 23912-87-0 ]
  • 8
  • [ 625-05-8 ]
  • [ 50841-47-9 ]
  • [ 96564-52-2 ]
  • 11
  • [ 84796-62-3 ]
  • [ 625-05-8 ]
  • 12
  • [ 138261-28-6 ]
  • [ 625-05-8 ]
  • 13
  • [ 625-05-8 ]
  • [ 3282-30-2 ]
  • [ 63879-05-0 ]
  • 14
  • [ 625-05-8 ]
  • [ 501-53-1 ]
  • [ 51219-55-7 ]
YieldReaction ConditionsOperation in experiment
46% Step A: Synthesis of 3-benzyloxycarbonylamino-3-methyl-butyric acid. 3-Amino-3-methylbutyric acid (2.40 g, 20.49 mmol) was dissolved in NaOH (2 M aq, 35 mL), the resulting mixture cooled to 0° C., and benzyl chloroformate (5.77 mL, 40.97 mmol) added. The reaction mixture was stirred vigorously at 0° C. for 1 h and at RT for 3 h. Et2O (50 mL) was then added, and the layers separated. The organic layer was discarded. The aqueous layer was acidified to pH 2, brine added, and the resulting mixture extracted with EtOAc. The combined organic extracts were dried over anhydrous Na2SO4, filtered and evaporated under reduced pressure to give 3-benzyloxycarbonylamino-3-methyl-butyric acid (2.33 g, 46percent yield) without further purification.
  • 15
  • [ 625-05-8 ]
  • [ 185525-59-1 ]
  • N-[1(R)-[(2,3-Dihydrospiro[1H-indene-1,4'-piperidin]-1'-yl)carbonyl]-2-(1H-indol-3-yl)ethyl]-3-amino-3-methylbutanamide [ No CAS ]
  • 16
  • [ 625-05-8 ]
  • [ 170726-53-1 ]
  • 3-{2-[3-(4-{Amino-[(E)-tert-butoxycarbonylimino]-methyl}-phenyl)-4,5-dihydro-isoxazol-5-yl]-acetylamino}-3-methyl-butyric acid [ No CAS ]
  • 17
  • [ 826-36-8 ]
  • Cr2O3-H2SO4 [ No CAS ]
  • [ 625-05-8 ]
  • [ 79948-19-9 ]
  • 18
  • sulfate diacetonamine [ No CAS ]
  • [ 625-05-8 ]
  • [ 62-57-7 ]
  • 21
  • 3-benzamino-3-methyl-butyric acid [ No CAS ]
  • [ 625-05-8 ]
  • 22
  • [ 7647-01-0 ]
  • [ 19805-83-5 ]
  • Sn [ No CAS ]
  • [ 625-05-8 ]
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