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[ CAS No. 26638-53-9 ] {[proInfo.proName]}

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Chemical Structure| 26638-53-9
Chemical Structure| 26638-53-9
Structure of 26638-53-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 26638-53-9 ]

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Product Details of [ 26638-53-9 ]

CAS No. :26638-53-9 MDL No. :MFCD07368146
Formula : C14H10ClNO3S Boiling Point : No data available
Linear Structure Formula :- InChI Key :RGOFXWXKWORKIP-UHFFFAOYSA-N
M.W : 307.75 Pubchem ID :14950938
Synonyms :

Calculated chemistry of [ 26638-53-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 20
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.07
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 79.83
TPSA : 62.83 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -6.21 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.06
Log Po/w (XLOGP3) : 2.77
Log Po/w (WLOGP) : 3.41
Log Po/w (MLOGP) : 1.93
Log Po/w (SILICOS-IT) : 2.34
Consensus Log Po/w : 2.5

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.94
Solubility : 0.0356 mg/ml ; 0.000116 mol/l
Class : Soluble
Log S (Ali) : -3.75
Solubility : 0.0554 mg/ml ; 0.00018 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.33
Solubility : 0.00146 mg/ml ; 0.00000473 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.91

Safety of [ 26638-53-9 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H317-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 26638-53-9 ]

* 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.

  • Downstream synthetic route of [ 26638-53-9 ]

[ 26638-53-9 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 26638-53-9 ]
  • [ 26723-60-4 ]
YieldReaction ConditionsOperation in experiment
95% Example 13-Chloro-6-methyldibenzo[c,/][1,2]thiazepin-11 (6W)-ol S,S-dioxideTo a solution of compound of Formula Il (62.5 g) in methanol (500 ml) was charged sodium borohydride (15.04 g) at 0-5 °C. The reaction mass was stirred for 30 minutes at 0-5 0C, and for 30-60 minutes at RT. After the completion of the starting material, the solid was filtered and washed with methanol. The solid compound was dried until constant weight to provide the title compound in 90-95percent yield.
  • 3
  • [ 26638-53-9 ]
  • [ 26638-66-4 ]
  • 4
  • [ 26638-53-9 ]
  • [ 141528-85-0 ]
  • 5
  • [ 26638-53-9 ]
  • [ 141528-86-1 ]
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Technical Information

? Alkyl Halide Occurrence ? Baeyer-Villiger Oxidation ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Chan-Lam Coupling Reaction ? Clemmensen Reduction ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? General Reactivity ? Grignard Reaction ? Halogenation ? Heat of Combustion ? Henry Nitroaldol Reaction ? Hiyama Cross-Coupling Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Kinetics of Alkyl Halides ? Kumada Cross-Coupling Reaction ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? Mannich Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Passerini Reaction ? Paternò-Büchi Reaction ? Petasis Reaction ? Peterson Olefination ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Alkyl Halides with Reducing Metals ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reformatsky Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Specialized Acylation Reagents-Ketenes ? Specialized Acylation Reagents-Vilsmeier Reagent ? Stille Coupling ? Stobbe Condensation ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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