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[ CAS No. 27829-72-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 27829-72-7
Chemical Structure| 27829-72-7
Structure of 27829-72-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 27829-72-7 ]

CAS No. :27829-72-7 MDL No. :MFCD00036541
Formula : C8H14O2 Boiling Point : -
Linear Structure Formula :- InChI Key :SJRXWMQZUAOMRJ-VOTSOKGWSA-N
M.W : 142.20 Pubchem ID :5364778
Synonyms :
Chemical Name :Ethyl (E)-hex-2-enoate

Calculated chemistry of [ 27829-72-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.62
Num. rotatable bonds : 5
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 41.38
TPSA : 26.3 ?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) : -5.55 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.6
Log Po/w (XLOGP3) : 2.28
Log Po/w (WLOGP) : 1.91
Log Po/w (MLOGP) : 1.85
Log Po/w (SILICOS-IT) : 1.74
Consensus Log Po/w : 2.07

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.83
Solubility : 2.11 mg/ml ; 0.0149 mol/l
Class : Very soluble
Log S (Ali) : -2.47
Solubility : 0.482 mg/ml ; 0.00339 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.62
Solubility : 3.4 mg/ml ; 0.0239 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.36

Safety of [ 27829-72-7 ]

Signal Word:Danger Class:3
Precautionary Statements:P210-P280-P370+P378-P403+P235-P501 UN#:3272
Hazard Statements:H225 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 27829-72-7 ]

* 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 [ 27829-72-7 ]

[ 27829-72-7 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 75-52-5 ]
  • [ 27829-72-7 ]
  • [ 128013-61-6 ]
YieldReaction ConditionsOperation in experiment
99.4% With 1,8-diazabicyclo[5.4.0]undec-7-ene; at 0 - 20℃; for 3h; 1.a. Synthesis of 3-nitromethyl-hexanoic acid ethyl ester (B)(A) (B)To a stirred solution of hex-2-enoic acid ethyl ester (A) (45Og, 3.164mol,leq) in nitromethane (858ml, 15.822 mol, 5 eq) cooled at O0C, is added dropwise, under nitrogen,481.8g (3.164 mol, leq.) of 1.8-diazabicyclo[5.4.0]undec-7-ene (DBU). The reaction mixture is allowed to react at room temperature for 3h and is quenched with a 6M aqueous hydrogen chloride solution to obtain pH = 4. The solution is extracted with diethyl ether (500ml + 2 x 300ml). The organic layers are dried with MgSpsi4, filtered and concentrated to obtain an oil residue (672.13g, HPLC purity = 78.9percent) which is purified by liquid EPO <DP n="24"/>chromatography eluting with dichloromethane. 639.4 Ig of 3-nitromethyl-hexanoic acid ethyl ester (B) are obtained (yield = 99.4percent).GC/MS : MH+ = 204
  • 2
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  • [ 53662-68-3 ]
  • 4
  • [ 1071-46-1 ]
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  • 5
  • [ 36678-63-4 ]
  • [ 123-72-8 ]
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  • 6
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  • [ 109-94-4 ]
  • [ 344881-72-7 ]
  • 7
  • [ 1116-61-6 ]
  • [ 31930-35-5 ]
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  • 10
  • [ 57475-10-2 ]
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  • 12
  • [ 67889-05-8 ]
  • [ 123-72-8 ]
  • [ 27829-72-7 ]
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