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[ CAS No. 4136-26-9 ] {[proInfo.proName]}

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Chemical Structure| 4136-26-9
Chemical Structure| 4136-26-9
Structure of 4136-26-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 4136-26-9 ]

CAS No. :4136-26-9 MDL No. :MFCD18072919
Formula : C13H16O3 Boiling Point : -
Linear Structure Formula :- InChI Key :KYEDLQFODOWDRO-UHFFFAOYSA-N
M.W : 220.26 Pubchem ID :138129
Synonyms :

Calculated chemistry of [ 4136-26-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.46
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 61.97
TPSA : 35.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.88 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.55
Log Po/w (XLOGP3) : 2.48
Log Po/w (WLOGP) : 2.57
Log Po/w (MLOGP) : 1.58
Log Po/w (SILICOS-IT) : 3.28
Consensus Log Po/w : 2.49

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.91
Solubility : 0.269 mg/ml ; 0.00122 mol/l
Class : Soluble
Log S (Ali) : -2.87
Solubility : 0.297 mg/ml ; 0.00135 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.14
Solubility : 0.0159 mg/ml ; 0.0000721 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.06

Safety of [ 4136-26-9 ]

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

Application In Synthesis of [ 4136-26-9 ]

* 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 [ 4136-26-9 ]

[ 4136-26-9 ] Synthesis Path-Upstream   1~10

  • 1
  • [ 51458-29-8 ]
  • [ 4136-26-9 ]
YieldReaction ConditionsOperation in experiment
77% With Celite; pyridinium chlorochromate In benzene at 85℃; for 1 h; Added to a solution of 2.6 g (about 13 mmol) of this oil in benzene (96 ml) were 13.7 g (64 mmol) of pyridinium chlorochromate and 31.8 g of Celite, and the mixture was stirred for 1 hour at 85° C. Insoluble materials were removed from the reaction mixture by suction filtration through Celite, and the residue on Celite was washed with diethyl ether and ethyl acetate. The filtrate and washings were combined and concentrated under reduced pressure. The resultant crude oil was purified by column chromatography on silica gel, thereby obtaining 2.1 g (yield: 77percent) of 5,6-dimethoxy-3,3-dimethylindan-1-one as a colorless oil.
Reference: [1] Patent: US6340682, 2002, B1, . Location in patent: Page column 43-44
  • 2
  • [ 91-16-7 ]
  • [ 541-47-9 ]
  • [ 4136-26-9 ]
Reference: [1] European Journal of Organic Chemistry, 2003, # 19, p. 3735 - 3743
  • 3
  • [ 83923-91-5 ]
  • [ 74-88-4 ]
  • [ 4136-26-9 ]
Reference: [1] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1982, # 9, p. 2013 - 2018
  • 4
  • [ 91-16-7 ]
  • [ 37637-88-0 ]
  • [ 4136-26-9 ]
Reference: [1] Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1988, vol. 27, # 1-12, p. 339 - 341
  • 5
  • [ 2231-66-5 ]
  • [ 4136-26-9 ]
Reference: [1] Journal of Organic Chemistry, 2005, vol. 70, # 4, p. 1316 - 1327
  • 6
  • [ 98910-57-7 ]
  • [ 4136-26-9 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1985, vol. 22, # 2, p. 363 - 368
  • 7
  • [ 90-05-1 ]
  • [ 4136-26-9 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1985, vol. 22, # 2, p. 363 - 368
  • 8
  • [ 3350-78-5 ]
  • [ 91-16-7 ]
  • [ 4136-26-9 ]
  • [ 41280-64-2 ]
Reference: [1] Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1984, vol. 39, # 12, p. 1801 - 1805
  • 9
  • [ 541-47-9 ]
  • [ 4136-26-9 ]
Reference: [1] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1982, # 9, p. 2013 - 2018
  • 10
  • [ 98910-54-4 ]
  • [ 74-88-4 ]
  • [ 4136-26-9 ]
  • [ 98910-59-9 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1985, vol. 22, # 2, p. 363 - 368
[2] Journal of Heterocyclic Chemistry, 1985, vol. 22, # 2, p. 363 - 368
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