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[ CAS No. 629-30-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 629-30-1
Chemical Structure| 629-30-1
Structure of 629-30-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 629-30-1 ]

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Product Details of [ 629-30-1 ]

CAS No. :629-30-1 MDL No. :MFCD00002987
Formula : C7H16O2 Boiling Point : -
Linear Structure Formula :HO(CH2)7OH InChI Key :SXCBDZAEHILGLM-UHFFFAOYSA-N
M.W : 132.20 Pubchem ID :12381
Synonyms :

Calculated chemistry of [ 629-30-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 6
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 38.09
TPSA : 40.46 ?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) : -6.52 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.9
Log Po/w (XLOGP3) : 0.83
Log Po/w (WLOGP) : 0.92
Log Po/w (MLOGP) : 0.96
Log Po/w (SILICOS-IT) : 1.19
Consensus Log Po/w : 1.16

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.79
Solubility : 21.6 mg/ml ; 0.163 mol/l
Class : Very soluble
Log S (Ali) : -1.26
Solubility : 7.23 mg/ml ; 0.0547 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.53
Solubility : 3.92 mg/ml ; 0.0296 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.38

Safety of [ 629-30-1 ]

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 [ 629-30-1 ]

* 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 [ 629-30-1 ]

[ 629-30-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1701-24-2 ]
  • [ 629-30-1 ]
  • [ 372-31-6 ]
  • [ 124467-00-1 ]
  • [ 1701-18-4 ]
YieldReaction ConditionsOperation in experiment
With aniline; In PPA; B2 (2E/Z, 4E) N-Isobutyl 3-methyl-11-(2-trifluoromethyl-4-quinolinyloxy)undeca-2,4-dienamide Starting from 2-trifluoromethyl-4-chloroquinoline and 1,7-heptanediol. Ethyl trifluoroacetoacetate (3.7 g) and aniline (1.8 ml) were reacted together in polyphosphoric acid according to Joullie et al, J. Med. Chem., 16, 134 (1973), to give 2-trifluoromethyl-4-hydroxyquinoline (1.8 g).
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