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[ CAS No. 120-13-8 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 120-13-8
Chemical Structure| 120-13-8
Chemical Structure| 120-13-8
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Quality Control of [ 120-13-8 ]

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Product Citations

Product Details of [ 120-13-8 ]

CAS No. :120-13-8 MDL No. :MFCD00016831
Formula : C11H14O4 Boiling Point : -
Linear Structure Formula :- InChI Key :XVNXRPVJRCYHEW-UHFFFAOYSA-N
M.W : 210.23 Pubchem ID :67112
Synonyms :

Calculated chemistry of [ 120-13-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 5
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 55.78
TPSA : 55.76 Ų

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) : -6.43 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.96
Log Po/w (XLOGP3) : 1.62
Log Po/w (WLOGP) : 1.72
Log Po/w (MLOGP) : 1.38
Log Po/w (SILICOS-IT) : 1.97
Consensus Log Po/w : 1.73

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.13
Solubility : 1.56 mg/ml ; 0.00741 mol/l
Class : Soluble
Log S (Ali) : -2.4
Solubility : 0.831 mg/ml ; 0.00395 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.84
Solubility : 0.302 mg/ml ; 0.00144 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.79

Safety of [ 120-13-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 120-13-8 ]

* 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 [ 120-13-8 ]

[ 120-13-8 ] Synthesis Path-Downstream   1~18

  • 1
  • [ 120-13-8 ]
  • [ 858843-15-9 ]
  • 2
  • [ 66488-86-6 ]
  • [ 120-13-8 ]
  • 3
  • [ 120-13-8 ]
  • [ 1484-85-1 ]
  • (4-ethoxy-3-methoxy-phenyl)-acetic acid homopiperonylamide [ No CAS ]
  • 4
  • [ 50-00-0 ]
  • [ 120-13-8 ]
  • [ 91790-54-4 ]
  • 5
  • [ 18855-52-2 ]
  • [ 120-25-2 ]
  • [ 120-13-8 ]
  • 6
  • [ 67-56-1 ]
  • [ 120-13-8 ]
  • [ 55761-07-4 ]
  • 7
  • [ 120-13-8 ]
  • [ 107-14-2 ]
  • Cyanomethyl (4-ethoxy-3-methoxyphenyl)acetate [ No CAS ]
  • 9
  • 2-phenyl-4-<3-methoxy-4-ethoxy-benzyliden>-Δ2-oxazolinone-(5) [ No CAS ]
  • [ 120-13-8 ]
  • 10
  • [ 120-13-8 ]
  • [ 113982-79-9 ]
  • 11
  • [ 120-13-8 ]
  • [ 114130-63-1 ]
  • 12
  • [ 120-13-8 ]
  • [ 171814-31-6 ]
  • 16
  • [ 120-13-8 ]
  • [ 872274-89-0 ]
  • 17
  • [ 120-13-8 ]
  • 1-(4-ethoxy-5-methoxy-2-nitro-benzyl)-6,7-dimethoxy-3,4-dihydro-isoquinoline [ No CAS ]
  • 18
  • [ 1014720-83-2 ]
  • [ 120-13-8 ]
  • [ 1015484-18-0 ]
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Technical Information

• Acetal Formation • Acids Combine with Acyl Halides to Produce Anhydrides • Acyl Chloride Hydrolysis • Amide Hydrolysis • Amide Hydrolysis • Anhydride Hydrolysis • Arndt-Eistert Homologation • Benzylic Oxidation • Birch Reduction • Birch Reduction of Benzene • Blanc Chloromethylation • Carbonation of Organometallics • Carboxylate Salt Formation • Carboxylic Acids React with Alcohols to Form Esters • Complete Benzylic Oxidations of Alkyl Chains • Complete Benzylic Oxidations of Alkyl Chains • Conversion of Amino with Nitro • Decarboxylation of Substituted Propanedioic • Deprotection of Cbz-Amino Acids • Deprotonation of Methylbenzene • Directing Electron-Donating Effects of Alkyl • Electrophilic Chloromethylation of Polystyrene • Esters Are Reduced by LiAlH4 to Give Alcohols • Esters Hydrolyze to Carboxylic Acids and Alcohols • Ether Synthesis by Oxymercuration-Demercuration • Ethers Synthesis from Alcohols with Strong Acids • Formation of an Amide from an Amine and a Carboxylic Acid • Formation of an Amide from an Amine and a Carboxylic Acid • Friedel-Crafts Alkylation of Benzene with Acyl Chlorides • Friedel-Crafts Alkylation of Benzene with Carboxylic Anhydrides • Friedel-Crafts Alkylation Using Alkenes • Friedel-Crafts Alkylations of Benzene Using Alkenes • Friedel-Crafts Alkylations Using Alcohols • Friedel-Crafts Reaction • Grignard Reagents Transform Esters into Alcohols • Groups that Withdraw Electrons Inductively Are Deactivating and Meta Directing • Halogenation of Benzene • Heat of Combustion • Hunsdiecker-Borodin Reaction • Hydrogenation to Cyclohexane • Hydrogenolysis of Benzyl Ether • Nitration of Benzene • Nitriles Hydrolyze to Carboxylic Acids • Nomenclature of Ethers • Nucleophilic Aromatic Substitution • Nucleophilic Aromatic Substitution with Amine • Oxidation of Aldehydes Furnishes Carboxylic Acids • Oxidation of Alkyl-substituted Benzenes Gives Aromatic Ketones • Oxidation of Primary Alcohols Furnishes Carboxylic Acids • Passerini Reaction • Peptide Bond Formation with DCC • Periodic Acid Degradation of Sugars • Preparation of Alkylbenzene • Preparation of Amines • Preparation of Carboxylic Acids • Preparation of Ethers • Primary Ether Cleavage with Strong Nucleophilic Acids • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Carboxylic Acids • Reactions of Ethers • Reduction of Carboxylic Acids by LiAlH4 • Reduction of Carboxylic Acids by Lithium Aluminum Hydride • Reduction of Carboxylic Acids by Lithium Aluminum Hydride • Reductive Removal of a Diazonium Group • Reverse Sulfonation——Hydrolysis • Ring Opening of Oxacyclopropane • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Sulfonation of Benzene • Synthesis of Alcohols from Tertiary Ethers • The Acylium Ion Attack Benzene to Form Phenyl Ketones • The Claisen Rearrangement • The Conversion of Carboxylic Acids into Acyl Halides • The Nitro Group Conver to the Amino Function • The Nucleophilic Opening of Oxacyclopropanes • Ugi Reaction • Vilsmeier-Haack Reaction
Historical Records

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