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[ CAS No. 1655-07-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1655-07-8
Chemical Structure| 1655-07-8
Structure of 1655-07-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1655-07-8 ]

CAS No. :1655-07-8 MDL No. :MFCD00001631
Formula : C9H14O3 Boiling Point : -
Linear Structure Formula :- InChI Key :FGSGHBPKHFDJOP-UHFFFAOYSA-N
M.W : 170.21 Pubchem ID :95543
Synonyms :

Calculated chemistry of [ 1655-07-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.78
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 44.75
TPSA : 43.37 ?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) : -6.33 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.81
Log Po/w (XLOGP3) : 1.42
Log Po/w (WLOGP) : 1.31
Log Po/w (MLOGP) : 0.9
Log Po/w (SILICOS-IT) : 1.82
Consensus Log Po/w : 1.45

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.59
Solubility : 4.36 mg/ml ; 0.0256 mol/l
Class : Very soluble
Log S (Ali) : -1.94
Solubility : 1.97 mg/ml ; 0.0116 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.68
Solubility : 3.55 mg/ml ; 0.0208 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.39

Safety of [ 1655-07-8 ]

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 [ 1655-07-8 ]

* 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 [ 1655-07-8 ]

[ 1655-07-8 ] Synthesis Path-Downstream   1~16

  • 1
  • [ 57508-48-2 ]
  • [ 1655-07-8 ]
  • [ 111655-66-4 ]
  • 2
  • [ 1655-07-8 ]
  • [ 119068-37-0 ]
  • [ 29569-79-7 ]
  • [ 61586-78-5 ]
  • [ 1655-06-7 ]
  • 5
  • [ 1004-38-2 ]
  • [ 1655-07-8 ]
  • [ 19191-79-8 ]
  • 6
  • [ 1004-38-2 ]
  • [ 1655-07-8 ]
  • 1,3-diamino-5,6,7,8-tetrahydro-2,9a,10-triazaanthracen-9-one [ No CAS ]
  • 2,4-diamino-5,6,7,8-tetrahydro-3,4a,10-triazaphenanthren-9-one [ No CAS ]
  • 7
  • [ 2406-90-8 ]
  • [ 1655-07-8 ]
  • 2,11-dichloro-7,8,9,10-tetrahydrothiazolo[5,4-a]acridine [ No CAS ]
  • 8
  • [ 104-21-2 ]
  • [ 1655-07-8 ]
  • ethyl 1-[(4-methoxyphenyl)methyl]-2-cyclohexanonecarboxylate [ No CAS ]
  • 11
  • [ 29608-05-7 ]
  • [ 1655-07-8 ]
  • C21H31N3O4 [ No CAS ]
  • 12
  • [ 145100-51-2 ]
  • [ 1655-07-8 ]
  • [ 122135-83-5 ]
  • 13
  • [ 1655-07-8 ]
  • [ 122135-83-5 ]
YieldReaction ConditionsOperation in experiment
With trifluoromethylsulfonic anhydride; N-ethyl-N,N-diisopropylamine; In 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran; Step 1: ethyl 2-[(trifluoromethyl)sulfonyl]oxy}cyclohex-1-ene-1-carboxylate To a solution of ethyl cyclohexanone-2-carboxylate (5.02 g, 29.5 mmol) in DCM (100 mL) cooled to -78 C. was added DIPEA (25.4 mL, 146 mmol) and then triflic anhydride (5.98 mL, 35.4 mmol) dropwise. The mixture was then warmed to r.t. and stirred overnight. The reaction was then quenched with aqueous citric acid and extracted with additional water. The organic layer was dried over Na2SO4 and the solvent was removed in vacuo. The crude product was purified on silica (100% DCM) to give the title product as an oil.
  • 14
  • [ 2028-85-5 ]
  • [ 1655-07-8 ]
  • [ 59514-18-0 ]
  • 15
  • [ 38980-96-0 ]
  • [ 1655-07-8 ]
  • [ 1285661-67-7 ]
  • 16
  • [ 1655-07-8 ]
  • [ 4187-59-1 ]
  • [ 4187-60-4 ]
  • [ 1655-06-7 ]
  • [ 1655-06-7 ]
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