Alternatived Products of [ 1750-42-1 ]
Product Details of [ 1750-42-1 ]
CAS No. : 1750-42-1
MDL No. : MFCD00038814
Formula :
C3 H4 N2 O
Boiling Point :
No data available
Linear Structure Formula : C3 H2 NO(NH2 )
InChI Key : -
M.W :
84.08
Pubchem ID : -
Synonyms :
Calculated chemistry of [ 1750-42-1 ] Expand+
Physicochemical Properties
Num. heavy atoms :
6
Num. arom. heavy atoms :
5
Fraction Csp3 :
0.0
Num. rotatable bonds :
0
Num. H-bond acceptors :
2.0
Num. H-bond donors :
1.0
Molar Refractivity :
20.91
TPSA :
52.05 ?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) :
-6.8 cm/s
Lipophilicity
Log Po/w (iLOGP) :
1.03
Log Po/w (XLOGP3) :
0.02
Log Po/w (WLOGP) :
0.26
Log Po/w (MLOGP) :
-0.72
Log Po/w (SILICOS-IT) :
0.42
Consensus Log Po/w :
0.2
Druglikeness
Lipinski :
0.0
Ghose :
None
Veber :
0.0
Egan :
0.0
Muegge :
2.0
Bioavailability Score :
0.55
Water Solubility
Log S (ESOL) :
-0.99
Solubility :
8.59 mg/ml ; 0.102 mol/l
Class :
Very soluble
Log S (Ali) :
-0.67
Solubility :
18.2 mg/ml ; 0.216 mol/l
Class :
Very soluble
Log S (SILICOS-IT) :
-0.77
Solubility :
14.3 mg/ml ; 0.17 mol/l
Class :
Soluble
Medicinal Chemistry
PAINS :
0.0 alert
Brenk :
0.0 alert
Leadlikeness :
1.0
Synthetic accessibility :
2.23
Application In Synthesis of [ 1750-42-1 ]
* 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 [ 1750-42-1 ]
1
[ 1750-42-1 ]
[ 6627-22-1 ]
[ 1097250-90-2 ]
Yield Reaction Conditions Operation in experiment
40%
With sodium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene;tris-(dibenzylideneacetone)dipalladium(0); In water; toluene; at 100℃; for 3h;
To compound 12.1 (0.16 g, 0.91 mmol, 1.0 equiv), isoxazol-3-ylamine (92 mg, 1.1 mmol, 1.2 equiv), tris(dibenzylideneacetone)-dipalladium (21 mg, 0.023 mmol, 0.025 equiv), xantphos (39 mg, 0.068 mmol, 0.075 equiv), and Na2CO3 (133 mg, 1.4 mmol, 1.4 equiv) in toluene (3 mL) was added H2O (16 μL, 0.91 mmol, 1.0 equiv). The reaction mixture was heated to 100 C. and stirred for 3 hr, whereupon it was cooled to RT. The mixture was filtered through Celite and adsorbed onto SiO2 gel. Purification by flash column chromatography (50-75-100% EtOAc/hexanes) afforded 12.2 (0.79 mg, 40%). LCMS: m/z: 221 [M+1]+.
2
[ 1750-42-1 ]
[ 2012-74-0 ]
[ 1208552-75-3 ]