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[ CAS No. 6683-48-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 6683-48-3
Chemical Structure| 6683-48-3
Structure of 6683-48-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 6683-48-3 ]

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Product Citations

Product Details of [ 6683-48-3 ]

CAS No. :6683-48-3 MDL No. :MFCD00833394
Formula : C15H22 Boiling Point : No data available
Linear Structure Formula :- InChI Key :AISXBZVAYNUAKB-UHFFFAOYSA-N
M.W : 202.34 Pubchem ID :81187
Synonyms :

Calculated chemistry of [ 6683-48-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.6
Num. rotatable bonds : 0
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 67.83
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -3.69 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.13
Log Po/w (XLOGP3) : 5.41
Log Po/w (WLOGP) : 4.34
Log Po/w (MLOGP) : 5.45
Log Po/w (SILICOS-IT) : 4.87
Consensus Log Po/w : 4.64

Druglikeness

Lipinski : 1.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -4.8
Solubility : 0.00322 mg/ml ; 0.0000159 mol/l
Class : Moderately soluble
Log S (Ali) : -5.17
Solubility : 0.00138 mg/ml ; 0.00000684 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.42
Solubility : 0.00076 mg/ml ; 0.00000376 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.84

Safety of [ 6683-48-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302-H312-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 6683-48-3 ]

* 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.

  • Upstream synthesis route of [ 6683-48-3 ]
  • Downstream synthetic route of [ 6683-48-3 ]

[ 6683-48-3 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 6683-48-3 ]
  • [ 153559-48-9 ]
Reference: [1] Journal of Organic Chemistry, 2001, vol. 66, # 17, p. 5772 - 5782
[2] Journal of Medicinal Chemistry, 1995, vol. 38, # 17, p. 3368 - 3383
[3] Journal of Labelled Compounds and Radiopharmaceuticals, 1995, vol. 36, # 7, p. 701 - 712
[4] Journal of Medicinal Chemistry, 1994, vol. 37, # 18, p. 2930 - 2941
[5] Patent: WO2011/103321, 2011, A1,
  • 2
  • [ 6683-48-3 ]
  • [ 1349659-56-8 ]
  • [ 1349659-57-9 ]
  • [ 153559-48-9 ]
Reference: [1] Patent: WO2011/141928, 2011, A1,
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Technical Information

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[ 6683-48-3 ]

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Chemical Structure| 169126-64-1

[ 169126-64-1 ]

(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)boronic acid

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[ 6683-48-3 ]

Chemical Structure| 1391053-02-3

A1267917[ 1391053-02-3 ]

1,1,4,4,6-Pentamethyl-1,2,3,4-tetrahydronaphthalene-13C4

Reason: Stable Isotope

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