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[ CAS No. 27538-10-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 27538-10-9
Chemical Structure| 27538-10-9
Structure of 27538-10-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 27538-10-9 ]

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Product Citations

Product Details of [ 27538-10-9 ]

CAS No. :27538-10-9 MDL No. :MFCD00191360
Formula : C7H10O3 Boiling Point : -
Linear Structure Formula :C2H5CHCOCOHCCH3O InChI Key :-
M.W : 142.15 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 27538-10-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.57
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 36.03
TPSA : 46.53 ?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) : -6.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.78
Log Po/w (XLOGP3) : 1.21
Log Po/w (WLOGP) : 1.15
Log Po/w (MLOGP) : -0.57
Log Po/w (SILICOS-IT) : 1.08
Consensus Log Po/w : 0.93

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -1.42
Solubility : 5.43 mg/ml ; 0.0382 mol/l
Class : Very soluble
Log S (Ali) : -1.78
Solubility : 2.34 mg/ml ; 0.0164 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.94
Solubility : 16.4 mg/ml ; 0.116 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.36

Safety of [ 27538-10-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 27538-10-9 ]

* 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 [ 27538-10-9 ]

[ 27538-10-9 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 80037-19-0 ]
  • [ 27538-10-9 ]
Reference: [1] Synthesis, 1981, # 9, p. 709
  • 2
  • [ 73920-09-9 ]
  • [ 27538-10-9 ]
Reference: [1] Synthesis, 1981, # 9, p. 709
  • 3
  • [ 87-72-9 ]
  • [ 56-41-7 ]
  • [ 3658-77-3 ]
  • [ 27538-10-9 ]
Reference: [1] Journal of Agricultural and Food Chemistry, 1996, vol. 44, # 2, p. 531 - 536
  • 4
  • [ 58-86-6 ]
  • [ 56-41-7 ]
  • [ 3658-77-3 ]
  • [ 27538-10-9 ]
Reference: [1] Journal of Agricultural and Food Chemistry, 2003, vol. 51, # 9, p. 2708 - 2713
  • 5
  • [ 58-86-6 ]
  • [ 56-40-6 ]
  • [ 3658-77-3 ]
  • [ 27538-10-9 ]
Reference: [1] Journal of Agricultural and Food Chemistry, 2003, vol. 51, # 9, p. 2708 - 2713
  • 6
  • [ 948557-13-9 ]
  • [ 27538-10-9 ]
Reference: [1] Journal of Agricultural and Food Chemistry, 2007, vol. 55, # 16, p. 6705 - 6711
[2] European Journal of Organic Chemistry, 2012, # 26, p. 4963 - 4968
  • 7
  • [ 87-72-9 ]
  • [ 56-41-7 ]
  • [ 27538-10-9 ]
Reference: [1] Journal of Agricultural and Food Chemistry, 1996, vol. 44, # 2, p. 531 - 536
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Technical Information

? Acyl Group Substitution ? Appel Reaction ? Baeyer-Villiger Oxidation ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Bouveault-Blanc Reduction ? Bucherer-Bergs Reaction ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Catalytic Hydrogenation ? Chugaev Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Corey-Kim Oxidation ? Dess-Martin Oxidation ? Ester Cleavage ? Fischer Indole Synthesis ? Grignard Reaction ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Jones Oxidation ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? Martin's Sulfurane Dehydrating Reagent ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mitsunobu Reaction ? Moffatt Oxidation ? Oxidation of Alcohols by DMSO ? Passerini Reaction ? Paternò-Büchi Reaction ? Petasis Reaction ? Peterson Olefination ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Alcohols ? Preparation of Aldehydes and Ketones ? Preparation of Amines ? Prins Reaction ? Reactions of Alcohols ? Reactions of Aldehydes and Ketones ? Reactions of Amines ? Reactions with Organometallic Reagents ? Reformatsky Reaction ? Ritter Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Sharpless Olefin Synthesis ? Specialized Acylation Reagents-Carbodiimides and Related Reagents ? Specialized Acylation Reagents-Ketenes ? Stobbe Condensation ? Swern Oxidation ? Tebbe Olefination ? Ugi Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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