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[ CAS No. 1700-37-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1700-37-4
Chemical Structure| 1700-37-4
Structure of 1700-37-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1700-37-4 ]

CAS No. :1700-37-4 MDL No. :MFCD00003367
Formula : C14H12O2 Boiling Point : No data available
Linear Structure Formula :CHOC6H4OCH2C6H5 InChI Key :JAICGBJIBWDEIZ-UHFFFAOYSA-N
M.W : 212.24 Pubchem ID :74342
Synonyms :

Calculated chemistry of [ 1700-37-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.07
Num. rotatable bonds : 4
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 62.81
TPSA : 26.3 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.29 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.37
Log Po/w (XLOGP3) : 3.25
Log Po/w (WLOGP) : 2.93
Log Po/w (MLOGP) : 2.6
Log Po/w (SILICOS-IT) : 3.57
Consensus Log Po/w : 2.94

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.49
Solubility : 0.068 mg/ml ; 0.00032 mol/l
Class : Soluble
Log S (Ali) : -3.48
Solubility : 0.0709 mg/ml ; 0.000334 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.01
Solubility : 0.00205 mg/ml ; 0.00000966 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.66

Safety of [ 1700-37-4 ]

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

Application In Synthesis of [ 1700-37-4 ]

* 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 [ 1700-37-4 ]

[ 1700-37-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 141-82-2 ]
  • [ 1700-37-4 ]
  • [ 122024-75-3 ]
YieldReaction ConditionsOperation in experiment
96% With piperidine; pyridine; at 120℃; for 3h; General procedure: To themixture of the corresponding aldehyde (2.52 g, 12.7 mmol) andmalonic acid (1.99 g, 19.1 mmol), dry pyridine (6.5 ml) and piperidine(0.2 ml) were successively added. The mixture was stirred at120 C for 3 h, cooled to 10 C and acidified with HCl (~14 ml) at 1:1ratio with cooling and stirring. After 30 min, the precipitate wasfiltered, washed 3 times with H2O (20 ml) and air dried. The yieldsof o-, m- and p-PhO-CA were 92, 91 and 96%, respectively.
  • 2
  • [ 1700-37-4 ]
  • [ 76-05-1 ]
  • [ 162167-97-7 ]
  • {1-[3-(benzyloxy)benzyl]piperidin-3-yl}methanamine bis(trifluoroacetate) salt [ No CAS ]
  • 3
  • [ 141-82-2 ]
  • [ 1700-37-4 ]
  • 3-amino-3-(3-(benzyloxy)phenyl)propanoic acid [ No CAS ]
  • [ 122024-75-3 ]
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