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[ CAS No. 28664-35-9 ] {[proInfo.proName]}

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Chemical Structure| 28664-35-9
Chemical Structure| 28664-35-9
Structure of 28664-35-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 28664-35-9 ]

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Product Citations

Product Details of [ 28664-35-9 ]

CAS No. :28664-35-9 MDL No. :MFCD00059957
Formula : C6H8O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :UNYNVICDCJHOPO-UHFFFAOYSA-N
M.W : 128.13 Pubchem ID :62835
Synonyms :

Calculated chemistry of [ 28664-35-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.5
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 31.22
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) : -6.8 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.34
Log Po/w (XLOGP3) : 0.39
Log Po/w (WLOGP) : 0.76
Log Po/w (MLOGP) : -0.11
Log Po/w (SILICOS-IT) : 0.77
Consensus Log Po/w : 0.63

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.88
Solubility : 16.9 mg/ml ; 0.132 mol/l
Class : Very soluble
Log S (Ali) : -0.93
Solubility : 14.9 mg/ml ; 0.117 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.52
Solubility : 38.9 mg/ml ; 0.303 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.76

Safety of [ 28664-35-9 ]

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

Application In Synthesis of [ 28664-35-9 ]

* 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 [ 28664-35-9 ]

[ 28664-35-9 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 142484-26-2 ]
  • [ 28664-35-9 ]
Reference: [1] Journal of Organic Chemistry, 1992, vol. 57, # 16, p. 4558 - 4560
  • 2
  • [ 142484-27-3 ]
  • [ 28664-35-9 ]
Reference: [1] Journal of Organic Chemistry, 1992, vol. 57, # 16, p. 4558 - 4560
  • 3
  • [ 87068-70-0 ]
  • [ 28664-35-9 ]
Reference: [1] Journal of Agricultural and Food Chemistry, 2008, vol. 56, # 5, p. 1606 - 1610
  • 4
  • [ 781658-23-9 ]
  • [ 28664-35-9 ]
  • [ 99506-67-9 ]
Reference: [1] Journal of Agricultural and Food Chemistry, 1996, vol. 44, # 7, p. 1851 - 1856
[2] Journal of Agricultural and Food Chemistry, 1996, vol. 44, # 7, p. 1851 - 1856
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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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