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[ CAS No. 619-21-6 ] {[proInfo.proName]}

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Chemical Structure| 619-21-6
Chemical Structure| 619-21-6
Structure of 619-21-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 619-21-6 ]

CAS No. :619-21-6 MDL No. :MFCD00039575
Formula : C8H6O3 Boiling Point : -
Linear Structure Formula :C6H4(CHO)CO2H InChI Key :UHDNUPHSDMOGCR-UHFFFAOYSA-N
M.W : 150.13 Pubchem ID :12077
Synonyms :

Calculated chemistry of [ 619-21-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 38.79
TPSA : 54.37 ?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) : -5.97 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.87
Log Po/w (XLOGP3) : 1.76
Log Po/w (WLOGP) : 1.2
Log Po/w (MLOGP) : 0.97
Log Po/w (SILICOS-IT) : 1.36
Consensus Log Po/w : 1.23

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.15
Solubility : 1.06 mg/ml ; 0.00706 mol/l
Class : Soluble
Log S (Ali) : -2.52
Solubility : 0.454 mg/ml ; 0.00302 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.7
Solubility : 2.99 mg/ml ; 0.0199 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 619-21-6 ]

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

Application In Synthesis of [ 619-21-6 ]

* 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 [ 619-21-6 ]

[ 619-21-6 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 619-21-6 ]
  • [ 3537-14-2 ]
  • [ 896116-35-1 ]
YieldReaction ConditionsOperation in experiment
In nitrobenzene; at 160℃; for 30h; 0.87 g 3-carboxybenzaldehyde and 0.866 g <strong>[3537-14-2]2,3-diamino-5-nitropyridine</strong> in 50 ml nitrobenzene were heated to 160 C. for 30 hrs. The mixture was cooled to room temperature and 200 ml ethyl acetate and 100 ml ethyl ether were added. The precipitated product was collected by filtration and dried. Yield 1.135 g
  • 2
  • [ 619-21-6 ]
  • [ 120-35-4 ]
  • 3-[(2-Methoxy-5-phenylcarbamoyl-phenylamino)-methyl]-benzoic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example 241 3-[(2-Methoxy-5-phenylcarbamoyl-phenylamino)-methyl]-benzoic acid The title compound has been made using the procedure of Example 50, but using 3-amino-4-methoxy-N-phenyl benzamide and 3-carboxybenzaldehyde as starting materials, which are commercially available from Aldrich; m.p. 210-212 C.
  • 3
  • [ 619-21-6 ]
  • [ 486460-21-3 ]
  • 3-(3-(trifluoromethyl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine-7-carbonyl)benzaldehyde [ No CAS ]
  • 4
  • [ 619-21-6 ]
  • [ 486460-21-3 ]
  • (Z)-3-oxo-2-(3-(3-(trifluoromethyl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine-7-carbonyl)benzylidene)-2,3-dihydrobenzofuran-7-carboxamide [ No CAS ]
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