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[ CAS No. 36840-85-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 36840-85-4
Chemical Structure| 36840-85-4
Structure of 36840-85-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 36840-85-4 ]

CAS No. :36840-85-4 MDL No. :MFCD00078444
Formula : C11H16O4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :XAMCLRBWHRRBCN-UHFFFAOYSA-N
M.W : 212.24 Pubchem ID :93195
Synonyms :

Calculated chemistry of [ 36840-85-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.45
Num. rotatable bonds : 10
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 56.61
TPSA : 52.6 ?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) : -5.99 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.97
Log Po/w (XLOGP3) : 2.26
Log Po/w (WLOGP) : 1.62
Log Po/w (MLOGP) : 1.66
Log Po/w (SILICOS-IT) : 2.41
Consensus Log Po/w : 2.18

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.92
Solubility : 2.55 mg/ml ; 0.012 mol/l
Class : Very soluble
Log S (Ali) : -3.0
Solubility : 0.212 mg/ml ; 0.000998 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.18
Solubility : 1.4 mg/ml ; 0.00658 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.1

Safety of [ 36840-85-4 ]

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

Application In Synthesis of [ 36840-85-4 ]

* 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 [ 36840-85-4 ]

[ 36840-85-4 ] Synthesis Path-Upstream   1~6

  • 1
  • [ 111-29-5 ]
  • [ 814-68-6 ]
  • [ 36840-85-4 ]
Reference: [1] European Journal of Medicinal Chemistry, 1981, vol. 16, # 6, p. 515 - 524
[2] Russian Journal of Organic Chemistry, 2013, vol. 49, # 11, p. 1690 - 1702[3] Zh. Org. Khim., 2013, vol. 49, # 11, p. 1707 - 1718,12
[4] Polymer, 2015, vol. 65, p. 45 - 54
  • 2
  • [ 590-92-1 ]
  • [ 111-29-5 ]
  • [ 36840-85-4 ]
YieldReaction ConditionsOperation in experiment
75% With triethylamine In toluene a)
1,5-Pentamethylene diacrylate
1,5-Pentanediol (15.6 g) was heated in refluxing toluene (500 ml) with 3-bromopropionic acid (50.5 g) and a trace of p-toluenesulphonic acid for 4 hours.
The cooled toluene solution was then washed with aqueous sodium acetate solution and treated with triethylamine (50 ml) at reflux.
The cooled reaction mixture was washed well with water to remove triethylamine and triethylamine hydrobromide and then the toluene was removed under reduced pressure.
The product, 1,5-pentamethylene diacrylate (24.0 g, 75percent yield) was obtained as a pale liquid by high vacuum distillation (b.p. 90°-95° C./0.1 mm Hg).
Reference: [1] Patent: US5453510, 1995, A,
  • 3
  • [ 111-29-5 ]
  • [ 292638-85-8 ]
  • [ 36840-85-4 ]
Reference: [1] Patent: WO2010/128518, 2010, A2, . Location in patent: Page/Page column 7; 10; 11
  • 4
  • [ 53219-90-2 ]
  • [ 36840-85-4 ]
Reference: [1] Journal of pharmaceutical sciences, 1974, vol. 63, # 7, p. 1162 - 1163
  • 5
  • [ 111-29-5 ]
  • [ 36840-85-4 ]
Reference: [1] Journal of pharmaceutical sciences, 1974, vol. 63, # 7, p. 1162 - 1163
  • 6
  • [ 111-29-5 ]
  • [ 292638-85-8 ]
  • [ 36840-85-4 ]
  • [ 57198-94-4 ]
Reference: [1] Journal of Molecular Catalysis B: Enzymatic, 2010, vol. 62, # 1, p. 80 - 89
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