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[ CAS No. 556-90-1 ] {[proInfo.proName]}

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Chemical Structure| 556-90-1
Chemical Structure| 556-90-1
Structure of 556-90-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 556-90-1 ]

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Product Details of [ 556-90-1 ]

CAS No. :556-90-1 MDL No. :MFCD00003186
Formula : C3H4N2OS Boiling Point : No data available
Linear Structure Formula :- InChI Key :-
M.W : 116.14 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 556-90-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.33
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 31.93
TPSA : 80.75 ?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) : -7.19 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.56
Log Po/w (XLOGP3) : -0.25
Log Po/w (WLOGP) : -0.81
Log Po/w (MLOGP) : -1.35
Log Po/w (SILICOS-IT) : 1.19
Consensus Log Po/w : -0.13

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.4
Solubility : 46.0 mg/ml ; 0.396 mol/l
Class : Very soluble
Log S (Ali) : -0.99
Solubility : 12.0 mg/ml ; 0.103 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.33
Solubility : 54.3 mg/ml ; 0.468 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.87

Safety of [ 556-90-1 ]

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 [ 556-90-1 ]

* 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 [ 556-90-1 ]

[ 556-90-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 556-90-1 ]
  • [ 31680-08-7 ]
  • 5-(4-methoxy-3-nitrobenzylidene)-2-iminothiazolidin-4-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
54% General procedure: To the magnetically stirred solution of 17 (232 mg, 2 mmol) in HOAc (7 mL), was added NaOAc (500 mg, 6 mmol). After 15 min 3,4-dimethoxybenzaldhyde (16a, 400 mg, 2.4 mmol) was added and the reaction mixture was heated under reflux for 72 h. The HOAc was removed under reduced pressure and the resultant solid was washed successively with water, methanol and EtOAc to obtain the desired products as solid. 10.2.1.6 5-(4-Methoxy-3-nitrobenzylidene)-2-iminothiazolidin-4-one (14f) Orange solid; mp > 200 C; 301 mg, 54% yield; IR (neat) νmax = 3236, 2951, 1682, 1608 cm-1; 1H NMR (400 MHz, CD3SOCD3) δ 9.49 (s, 1H), 9.21 (s, 1H), 8.11 (s, 1H), 7.86 (d, J = 8.00 1H), 7.58 (s, 1H) 7.51 (d, J = 8.84, 1H) 4.31 (s, 3H); 13C NMR (100 MHz, CD3SOCD3): δ 180.62, 175.61, 153.00, 139.71, 135.70, 130.05, 127.13, 125.98, 115.70, 57.51: HRMS (ESI-TOF): m/z calculated for C11H9N3O4S [M+Na]+, 302.0211; found 302.0244.
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