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[ CAS No. 4437-51-8 ] {[proInfo.proName]}

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Chemical Structure| 4437-51-8
Chemical Structure| 4437-51-8
Structure of 4437-51-8 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Citations

Jeremy J. Roos ; Prakhar Gautam ; Maximilian P. Martin , et al. DOI:

Abstract: The syntheses and characterization of Fe and Co complexes supported by a new tetra-imine macrocycle, TEIM (2,3,9,10-tetraethyl-1,4,8,11-tetraazacyclotetradeca-1,3,8,10-tetraene), are reported. Templating with Co(OAc)2·4H2O yielded trans-[Co(TEIM)Cl2][PF6] (1a), which was converted to trans-[Co(TEIM)X2][PF6] (X?=?N3 (2a) and NO2 (3a)) through reactions with NaX (X?=?N3 or NO2). Templating with Fe generated trans-[Fe(TEIM)(NCCH3)2][PF6]2, which was oxidized to trans-[Fe(TEIM)Cl2][PF6] (1b). The reaction of 1b with NaN3 formed [Fe(TEIM)(N3)2][PF6] (2b) while the reaction with [Fe(TEIM)(NCCH3)2][PF6]2 and NaNO2 yielded trans-[Fe(TEIM)(NO2)2] (3b). Single crystal X-ray diffraction studies revealed a pseudo-octahedral geometry around the Co / Fe centers with the ethyl groups oriented above or below the plane of the TEIM ring. The absorption spectra of 1b displays weak charge transfer bands near the UV to visible region, while 2b and 3b displayed intense charge transfer bands within the visible region. Cyclic voltammograms of 1a revealed four 1 e? reductions while those of 2a and 3a display only three cathodically shifted reductions. Analogous studies of 1b and 2b revealed two 1 e- reductions while 3b displays only an oxidation event. EPR studies of ferric complexes 1b and 2b indicated a low spin d5 electronic figuration with S?=?? ground state.

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Product Details of [ 4437-51-8 ]

CAS No. :4437-51-8 MDL No. :MFCD00010237
Formula : C6H10O2 Boiling Point : No data available
Linear Structure Formula :C2H5C(O)C(O)C2H5 InChI Key :KVFQMAZOBTXCAZ-UHFFFAOYSA-N
M.W : 114.14 Pubchem ID :62539
Synonyms :

Calculated chemistry of [ 4437-51-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.67
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 31.36
TPSA : 34.14 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.62 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.76
Log Po/w (XLOGP3) : 0.53
Log Po/w (WLOGP) : 0.94
Log Po/w (MLOGP) : 0.35
Log Po/w (SILICOS-IT) : 1.08
Consensus Log Po/w : 0.93

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.68
Solubility : 23.7 mg/ml ; 0.207 mol/l
Class : Very soluble
Log S (Ali) : -0.82
Solubility : 17.4 mg/ml ; 0.152 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.3
Solubility : 5.67 mg/ml ; 0.0497 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 4437-51-8 ]

Signal Word:Danger Class:3
Precautionary Statements:P210-P233-P240-P241+P242+P243-P280-P303+P361+P353-P370+P378-P403+P235-P501 UN#:1224
Hazard Statements:H225 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 4437-51-8 ]

* 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 [ 4437-51-8 ]

[ 4437-51-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 13754-19-3 ]
  • [ 4437-51-8 ]
  • 6,7-diethyl-pteridine [ No CAS ]
  • 3
  • [ 497-06-3 ]
  • copper [ No CAS ]
  • [ 4437-51-8 ]
  • [ 123-38-6 ]
  • [ 5077-67-8 ]
  • [ 123-73-9 ]
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