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[ CAS No. 1219960-66-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1219960-66-3
Chemical Structure| 1219960-66-3
Structure of 1219960-66-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1219960-66-3 ]

CAS No. :1219960-66-3 MDL No. :MFCD13559827
Formula : C9H15NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :CWSSMKIHNJENMC-UHFFFAOYSA-N
M.W : 185.22 Pubchem ID :20132023
Synonyms :

Calculated chemistry of [ 1219960-66-3 ]

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.78
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 48.07
TPSA : 66.4 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) : -6.92 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.67
Log Po/w (XLOGP3) : 0.72
Log Po/w (WLOGP) : 0.77
Log Po/w (MLOGP) : 0.45
Log Po/w (SILICOS-IT) : 0.59
Consensus Log Po/w : 0.84

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -1.18
Solubility : 12.3 mg/ml ; 0.0664 mol/l
Class : Very soluble
Log S (Ali) : -1.69
Solubility : 3.76 mg/ml ; 0.0203 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.96
Solubility : 20.4 mg/ml ; 0.11 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.49

Safety of [ 1219960-66-3 ]

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 [ 1219960-66-3 ]

* 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.

  • Downstream synthetic route of [ 1219960-66-3 ]

[ 1219960-66-3 ] Synthesis Path-Downstream   1~1

YieldReaction ConditionsOperation in experiment
55. 2-Methylalanine derivatives. 55-1. N-propionyl-2-methylalanine 55-2. N-benzoyl-2-methylalanine 55-3. N-(m-toluoyl)-2-methylalanine 55-4. N-(3-methoxybenzoyl)-2-methylalanine 55-5. N-cyclobutanecarbonyl-2-methylalanine 55-6. N-phenylacetyl-2-methylalanine 55-7. N-phenethyloxycarbonyl-2-methylalanine 56-1. N-valeryl-2-methylserine 56-2. N-octanoyl-2-methylserine ...
52. 2-Methylalanine derivatives. 52-1. N -propionyl-2-methylalanine 52-2. N -benzoyl-2-methylalanine 52-3. N -(m -toluoyl)-2-methylalanine 52-4. N -(3-methoxybenzoyl)-2-methylalanine 52-5. N -cyclobutanecarbonyl-2-methylalanine 52-6. N -phenylacetyl-2-methylalanine 52-7. N -phenethyloxycarbonyl-2-methylalanine
50-20. N -benzoylglycylglyclhistidine ... 52-1. N -propionyl-2-methylalanine 52-2. N -benzoyl-2-methylalanine 52-3. N -(m -toluoyl)-2-methylalanine 52-4. N -(3-methoxybenzoyl)-2-methylalanine 52-5. N -cyclobutanecarbonyl-2-methylalanine 52-6. N -phenylacetyl-2-methylalanine 52-7. N -phenethyloxycarbonyl-2-methylalanine
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