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[ CAS No. 4985-46-0 ] {[proInfo.proName]}

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Chemical Structure| 4985-46-0
Chemical Structure| 4985-46-0
Structure of 4985-46-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 4985-46-0 ]

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Product Details of [ 4985-46-0 ]

CAS No. :4985-46-0 MDL No. :MFCD00069935
Formula : C9H12N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :PQFMNVGMJJMLAE-QMMMGPOBSA-N
M.W : 180.20 Pubchem ID :151243
Synonyms :

Calculated chemistry of [ 4985-46-0 ]      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 : 3.0
Molar Refractivity : 48.66
TPSA : 89.34 ?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) : -7.85 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.94
Log Po/w (XLOGP3) : -0.63
Log Po/w (WLOGP) : -0.25
Log Po/w (MLOGP) : 0.11
Log Po/w (SILICOS-IT) : 0.15
Consensus Log Po/w : 0.06

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.7
Solubility : 35.6 mg/ml ; 0.198 mol/l
Class : Very soluble
Log S (Ali) : -0.77
Solubility : 30.4 mg/ml ; 0.168 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.5
Solubility : 5.63 mg/ml ; 0.0313 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.58

Safety of [ 4985-46-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 4985-46-0 ]

* 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 [ 4985-46-0 ]

[ 4985-46-0 ] Synthesis Path-Downstream   1~20

  • 1
  • [ 515-84-4 ]
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  • [ 116055-06-2 ]
  • 3
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  • <i>S</i>-Benzyl-<i>N</i>-benzyloxycarbonyl-L-cysteinylazid [ No CAS ]
  • [ 96113-36-9 ]
  • 5
  • [ 4985-46-0 ]
  • [ 541-41-3 ]
  • [ 7377-01-7 ]
  • 6
  • [ 3417-91-2 ]
  • [ 4985-46-0 ]
YieldReaction ConditionsOperation in experiment
86% With ammonium hydroxide; at 20℃; for 4h; L-tyrosine methyl ester hydrochloride (1.16 g, 5 mmol) and concentrated aqueous ammonia (40 mL) were added to a 50 ml reaction vessel and stirred for 4 h at room temperature. Rotary evaporation of ammonia, spin dry, with anhydrous ethanol (20mL × 2) with water, column chromatography (silica gel, 200-300 mesh; exhibition Preparative, ethyl acetate: methanol: aqueous ammonia = 300: 10: 15) gave L-tyrosinamide in 86% yield.
  • 7
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  • [ 79-04-9 ]
  • [ 7376-98-9 ]
  • 8
  • [ 4985-46-0 ]
  • [ 67-64-1 ]
  • <i>N</i>-isopropylidene-L-tyrosine amide [ No CAS ]
  • 9
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  • [ 407-25-0 ]
  • [ 7376-99-0 ]
  • 10
  • [ 4985-46-0 ]
  • [ 25830-77-7 ]
  • <i>N</i>-(<i>N</i>,<i>N</i>-phthaloyl-L-γ-glutamyl)-L-tyrosin-amide [ No CAS ]
  • 11
  • [ 4985-46-0 ]
  • [ 942-91-6 ]
  • [ 15985-81-6 ]
  • 12
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  • [ 52999-90-3 ]
  • [ 15985-84-9 ]
  • 13
  • [ 2419-54-7 ]
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  • [ 22839-98-1 ]
  • 14
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  • [ 7635-36-1 ]
  • [ 17193-61-2 ]
  • 15
  • [ 1943-83-5 ]
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  • (S)-2-[3-(2-Chloro-ethyl)-ureido]-3-(4-hydroxy-phenyl)-propionamide [ No CAS ]
  • 16
  • [ 1145-80-8 ]
  • [ 4985-46-0 ]
  • [ 114519-10-7 ]
  • 17
  • [ 7685-65-6 ]
  • [ 4985-46-0 ]
  • [ 95311-14-1 ]
  • 19
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  • [ 78330-94-6 ]
  • [ 78700-70-6 ]
  • 20
  • [ 4985-46-0 ]
  • C33H44N4O10 [ No CAS ]
  • [ 78700-70-6 ]
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Reason: Free-salt

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