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[ CAS No. 96-26-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 96-26-4
Chemical Structure| 96-26-4
Structure of 96-26-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 96-26-4 ]

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Product Citations

Product Details of [ 96-26-4 ]

CAS No. :96-26-4 MDL No. :MFCD00004670
Formula : C3H6O3 Boiling Point : -
Linear Structure Formula :OHCH2C(O)CH2OH InChI Key :RXKJFZQQPQGTFL-UHFFFAOYSA-N
M.W : 90.08 Pubchem ID :670
Synonyms :

Calculated chemistry of [ 96-26-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 6
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.67
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 19.06
TPSA : 57.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.82 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.48
Log Po/w (XLOGP3) : -1.36
Log Po/w (WLOGP) : -1.46
Log Po/w (MLOGP) : -1.66
Log Po/w (SILICOS-IT) : -0.63
Consensus Log Po/w : -0.93

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : 0.59
Solubility : 351.0 mg/ml ; 3.89 mol/l
Class : Highly soluble
Log S (Ali) : 0.65
Solubility : 404.0 mg/ml ; 4.49 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : 0.61
Solubility : 366.0 mg/ml ; 4.06 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 96-26-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 96-26-4 ]

* 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.

  • Downstream synthetic route of [ 96-26-4 ]

[ 96-26-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 497-09-6 ]
  • [ 96-26-4 ]
  • [ 20880-92-6 ]
  • 2
  • [ 96-26-4 ]
  • [ 38993-84-9 ]
YieldReaction ConditionsOperation in experiment
32% With methylamine hydrochloride; 31-1) 5-Hydroxymethyl-1-methylimidazole The title compound was obtained in a yield of 32percent according to the procedure described in J. M. Dener, L-H Zhang, H. Rapoport, J. Org. Chem., 1993, 58, 1159 using dihydroxyacetone and methylamine hydrochloride as starting materials. 1H NMR(CDCl3) delta3.67(s, 3H), 4.58(s, 2H), 5.37(brs, 1H), 6.76(s, 1H), 7.32(s, 1H)
  • 3
  • [ 497-09-6 ]
  • [ 96-26-4 ]
  • [ 87-79-6 ]
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Technical Information

? Alkyl Halide Occurrence ? Appel Reaction ? Baeyer-Villiger Oxidation ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Bucherer-Bergs Reaction ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Chugaev Reaction ? Clemmensen Reduction ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Corey-Kim Oxidation ? Dess-Martin Oxidation ? Fischer Indole Synthesis ? Grignard Reaction ? Halogenation ? Heat of Combustion ? 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 ? Nucleophilicity of Organophosphorus Compounds ? Organophosphorus Compounds as Reducing Agents ? Oxidation of Alcohols by DMSO ? Oxidation States of Organophosphorus Compounds ? 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 of Phosphorus and Sulfur Ylides ? Reactions with Organometallic Reagents ? Reformatsky Reaction ? Ritter Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Sharpless Olefin Synthesis ? Specialized Acylation Reagents-Ketenes ? Stobbe Condensation ? Swern Oxidation ? Tebbe Olefination ? Ugi Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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