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[ CAS No. 3328-69-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 3328-69-6
Chemical Structure| 3328-69-6
Structure of 3328-69-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 3328-69-6 ]

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Product Citations

Product Details of [ 3328-69-6 ]

CAS No. :3328-69-6 MDL No. :MFCD00839420
Formula : C8H6O3 Boiling Point : -
Linear Structure Formula :- InChI Key :JJOPQMAMJLOGFB-UHFFFAOYSA-N
M.W : 150.13 Pubchem ID :345554
Synonyms :
Chemical Name :2-Hydroxyisophthalaldehyde

Calculated chemistry of [ 3328-69-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 39.24
TPSA : 54.37 ?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) : -6.48 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.72
Log Po/w (XLOGP3) : 1.04
Log Po/w (WLOGP) : 1.02
Log Po/w (MLOGP) : 0.15
Log Po/w (SILICOS-IT) : 1.65
Consensus Log Po/w : 0.92

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.7
Solubility : 3.01 mg/ml ; 0.0201 mol/l
Class : Very soluble
Log S (Ali) : -1.77
Solubility : 2.54 mg/ml ; 0.0169 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.7
Solubility : 2.99 mg/ml ; 0.0199 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 3328-69-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313 UN#:N/A
Hazard Statements:H315-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 3328-69-6 ]

* 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 [ 3328-69-6 ]

[ 3328-69-6 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 610-04-8 ]
  • [ 3328-69-6 ]
  • 4
  • [ 930-68-7 ]
  • [ 109-94-4 ]
  • [ 3328-69-6 ]
  • [ 15329-04-1 ]
  • 5
  • [ 67-66-3 ]
  • [ 108-95-2 ]
  • [ 3328-69-6 ]
  • [ 3328-70-9 ]
  • [ 123-08-0 ]
  • [ 90-02-8 ]
  • 6
  • [ 110-52-1 ]
  • [ 3328-69-6 ]
  • 1,4-di(2,6-diformylphenoxy)butane [ No CAS ]
  • 7
  • [ 3328-69-6 ]
  • [ 96948-23-1 ]
  • 2,6-Bis-[(E)-(S)-1-benzyl-pyrrolidin-2-ylmethylimino]-methyl}-phenol [ No CAS ]
  • 9
  • [ 3328-69-6 ]
  • [ 137605-43-7 ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 11 9.0 Parts of the product of Example 10 were added rapidly to a refluxing solution of hexamine (20.0 parts in tetrachloroethylene (250 parts by volume). A white solid rapidly precipitated. After refluxing for 1 hour the solid was filtered off and added to 150 parts by volume of 60% by volume aqueous ethyl alcohol. After refluxing for 0.5 hours, 25 parts by volume of concentrated hydrochloric acid was added and the refluxing continued for a further 0.1 hours. The product was isolated by steam distillation and ether extraction of the distillate to give 0.1 parts of 2-hydroxyisophthalaldehyde, m.pt. 122-125 C.
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Technical Information

? Acidity of Phenols ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Chan-Lam Coupling Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Chaykovsky Reaction ? Corey-Fuchs Reaction ? Electrophilic Substitution of the Phenol Aromatic Ring ? Etherification Reaction of Phenolic Hydroxyl Group ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? Grignard Reaction ? Halogenation of Phenols ? Hantzsch Dihydropyridine Synthesis ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Julia-Kocienski Olefination ? Knoevenagel Condensation ? Leuckart-Wallach Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mukaiyama Aldol Reaction ? Nozaki-Hiyama-Kishi Reaction ? Oxidation of Phenols ? Passerini Reaction ? Paternò-Büchi Reaction ? Pechmann Coumarin Synthesis ? Petasis Reaction ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reformatsky Reaction ? Reimer-Tiemann Reaction ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Stetter Reaction ? Stobbe Condensation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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