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[ CAS No. 1779-49-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 1779-49-3
Chemical Structure| 1779-49-3
Structure of 1779-49-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1779-49-3 ]

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Product Citations

Product Citations

Shashwati Paul ; Daniel Adelfinsky ; Christophe Salome , et al. DOI:

Abstract: Identification of rigid counterparts for common flexible scaffolds is crucial to the advancement of medicinal chemistry. Here we showcase a new class of building blocks, 2,5-disubstituted bicyclo[2.1.1]hexanes that can act as rigidified cis-, or trans-1,3-disubstituted cyclopentanes, common motifs in drugs. The scalable synthesis of these structures was enabled through the use of C–H functionalization logic and cycloaddition reactions.

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Product Details of [ 1779-49-3 ]

CAS No. :1779-49-3 MDL No. :MFCD00011804
Formula : C19H18BrP Boiling Point : -
Linear Structure Formula :CH3(C6H5)3PBr InChI Key :LSEFCHWGJNHZNT-UHFFFAOYSA-M
M.W : 357.22 Pubchem ID :74505
Synonyms :

Calculated chemistry of [ 1779-49-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 21
Num. arom. heavy atoms : 18
Fraction Csp3 : 0.05
Num. rotatable bonds : 3
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 99.94
TPSA : 13.59 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.38 cm/s

Lipophilicity

Log Po/w (iLOGP) : -1.74
Log Po/w (XLOGP3) : 4.37
Log Po/w (WLOGP) : 0.61
Log Po/w (MLOGP) : 5.74
Log Po/w (SILICOS-IT) : 4.74
Consensus Log Po/w : 2.74

Druglikeness

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

Water Solubility

Log S (ESOL) : -5.24
Solubility : 0.00204 mg/ml ; 0.0000057 mol/l
Class : Moderately soluble
Log S (Ali) : -4.37
Solubility : 0.0152 mg/ml ; 0.0000425 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -7.93
Solubility : 0.0000042 mg/ml ; 0.0000000117 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 4.5

Safety of [ 1779-49-3 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P264-P270-P271-P301+P310-P304+P340-P312-P330-P403+P233-P405-P501 UN#:2811
Hazard Statements:H301-H411 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1779-49-3 ]

* 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 [ 1779-49-3 ]
  • Downstream synthetic route of [ 1779-49-3 ]

[ 1779-49-3 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 1779-49-3 ]
  • [ 153559-45-6 ]
  • [ 153559-48-9 ]
YieldReaction ConditionsOperation in experiment
66% With sodium amide In tetrahydrofuran Rectangular plates of compound 35 were found suitable for X-ray diffraction, and a study was conducted. To complete the synthesis of bexarotene, the Friedel-Crafts acylation of 35, by crude mono-methyl-terephthaloyl chloride (36), gave ketone (37) which was converted to alkene ester(38) by a Wittig reaction, and ester 38 was saponified by potassium hydroxide followed by acidification with aqueous hydrochloric acid to give bexarotene (39) (Scheme 2).
Reference: [1] Journal of Medicinal Chemistry, 2009, vol. 52, # 19, p. 5950 - 5966
[2] Patent: WO2011/103321, 2011, A1, . Location in patent: Page/Page column 19
[3] Journal of Medicinal Chemistry, 1994, vol. 37, # 18, p. 2930 - 2941
[4] Journal of Labelled Compounds and Radiopharmaceuticals, 1995, vol. 36, # 7, p. 701 - 712
[5] Journal of Medicinal Chemistry, 1995, vol. 38, # 17, p. 3368 - 3383
  • 2
  • [ 1779-49-3 ]
  • [ 153559-45-6 ]
  • [ 1349659-53-5 ]
  • [ 1349659-55-7 ]
  • [ 1349659-56-8 ]
  • [ 1349659-57-9 ]
  • [ 153559-48-9 ]
Reference: [1] Patent: WO2011/141928, 2011, A1, . Location in patent: Page/Page column 19
  • 3
  • [ 1779-49-3 ]
  • [ 98977-36-7 ]
  • [ 276872-89-0 ]
Reference: [1] European Journal of Medicinal Chemistry, 2011, vol. 46, # 12, p. 5790 - 5799
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