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[ CAS No. 66799-93-7 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 66799-93-7
Chemical Structure| 66799-93-7
Chemical Structure| 66799-93-7
Structure of 66799-93-7 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 66799-93-7 ]

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Product Citations

Product Details of [ 66799-93-7 ]

CAS No. :66799-93-7 MDL No. :MFCD06496489
Formula : C8H5BrO4 Boiling Point : -
Linear Structure Formula :- InChI Key :HLQBEIBAXJNCPT-UHFFFAOYSA-N
M.W : 245.03 Pubchem ID :4739141
Synonyms :

Calculated chemistry of [ 66799-93-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.16
TPSA : 55.76 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.41 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.74
Log Po/w (XLOGP3) : 1.95
Log Po/w (WLOGP) : 1.88
Log Po/w (MLOGP) : 1.49
Log Po/w (SILICOS-IT) : 1.93
Consensus Log Po/w : 1.8

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.86
Solubility : 0.336 mg/ml ; 0.00137 mol/l
Class : Soluble
Log S (Ali) : -2.75
Solubility : 0.44 mg/ml ; 0.0018 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.38
Solubility : 1.02 mg/ml ; 0.00415 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.26

Safety of [ 66799-93-7 ]

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 [ 66799-93-7 ]

* 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 [ 66799-93-7 ]

[ 66799-93-7 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 19522-96-4 ]
  • [ 66799-93-7 ]
  • 2
  • [ 67-56-1 ]
  • [ 66799-93-7 ]
  • [ 103095-80-3 ]
  • 4
  • [ 16414-34-9 ]
  • [ 66799-93-7 ]
  • 5
  • [ 66799-93-7 ]
  • [ 18107-18-1 ]
  • [ 103095-80-3 ]
  • 6
  • [ 66799-93-7 ]
  • (R)-7-(7-chloro-10-(3-(4-chloro-3,5-dimethylphenoxy)propyl)-4-methyl-1-oxo-6-(1,3,5-trimethyl-1H-pyrazol-4-yl)-3,4-dihydropyrazino[1,2-a]indol-2(1H)-yl)benzo[d][1,3]dioxole-5-carboxylic acid [ No CAS ]
  • 7
  • [ 66799-93-7 ]
  • methyl 7-iodobenzo[d][1,3]dioxole-5-carboxylate [ No CAS ]
  • 8
  • [ 66799-93-7 ]
  • C38H38Cl2N4O6 [ No CAS ]
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Technical Information

• Acid-Catalyzed α -Halogenation of Ketones • Acids Combine with Acyl Halides to Produce Anhydrides • Acyl Chloride Hydrolysis • Addition of a Hydrogen Halide to an Internal Alkyne • Alcohols from Haloalkanes by Acetate Substitution-Hydrolysis • Alcohols React with PX3 • Alkyl Halide Occurrence • Alkylation of an Alkynyl Anion • Amide Hydrolysis • Amide Hydrolysis • An Alkane are Prepared from an Haloalkane • Anhydride Hydrolysis • Arndt-Eistert Homologation • Carbonation of Organometallics • Carboxylate Salt Formation • Carboxylic Acids React with Alcohols to Form Esters • Convert Haloalkanes into Alcohols by SN2 • Decarboxylation of Substituted Propanedioic • Deprotection of Cbz-Amino Acids • Esters Hydrolyze to Carboxylic Acids and Alcohols • 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 Haloalkanes • General Reactivity • Grignard Reaction • Halogenation of Alkenes • Hiyama Cross-Coupling Reaction • Hunsdiecker-Borodin Reaction • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Methylation of Ammonia • Methylation of Ammonia • Nitriles Hydrolyze to Carboxylic Acids • Oxidation of Aldehydes Furnishes Carboxylic Acids • Oxidation of Primary Alcohols Furnishes Carboxylic Acids • Passerini Reaction • Peptide Bond Formation with DCC • Periodic Acid Degradation of Sugars • Preparation of Amines • Preparation of Carboxylic Acids • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Carboxylic Acids • Reactions of Dihalides • Reduction of Carboxylic Acids by LiAlH4 • Reduction of Carboxylic Acids by Lithium Aluminum Hydride • Reduction of Carboxylic Acids by Lithium Aluminum Hydride • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Stille Coupling • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • The Conversion of Carboxylic Acids into Acyl Halides • Ugi Reaction • Williamson Ether Syntheses
Historical Records

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