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[ CAS No. 98-71-5 ] {[proInfo.proName]}

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Chemical Structure| 98-71-5
Chemical Structure| 98-71-5
Structure of 98-71-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 98-71-5 ]

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Product Details of [ 98-71-5 ]

CAS No. :98-71-5 MDL No. :MFCD00025097
Formula : C6H8N2O3S Boiling Point : -
Linear Structure Formula :- InChI Key :IOMZCWUHFGMSEJ-UHFFFAOYSA-N
M.W : 188.20 Pubchem ID :66825
Synonyms :
Chemical Name :4-Hydrazinylbenzenesulfonic acid

Calculated chemistry of [ 98-71-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 3.0
Molar Refractivity : 43.51
TPSA : 100.8 ?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) : -10.66 cm/s

Lipophilicity

Log Po/w (iLOGP) : -0.19
Log Po/w (XLOGP3) : -4.52
Log Po/w (WLOGP) : 1.11
Log Po/w (MLOGP) : 0.49
Log Po/w (SILICOS-IT) : -1.24
Consensus Log Po/w : -0.87

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : 1.6
Solubility : 7540.0 mg/ml ; 40.1 mol/l
Class : Highly soluble
Log S (Ali) : 3.02
Solubility : 198000.0 mg/ml ; 1050.0 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -1.44
Solubility : 6.8 mg/ml ; 0.0361 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.05

Safety of [ 98-71-5 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338-P304+P340-P405-P501 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 98-71-5 ]

* 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 [ 98-71-5 ]

[ 98-71-5 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 527-69-5 ]
  • [ 24686-78-0 ]
  • [ 98-71-5 ]
  • 2-benzoyl-5-(furan-2-carbonyl)-2,3,4,5-tetrahydro-1<i>H</i>-pyrido[4,3-<i>b</i>]indole-8-sulfonic acid [ No CAS ]
  • 2
  • [ 24686-78-0 ]
  • [ 122-01-0 ]
  • [ 98-71-5 ]
  • 2-benzoyl-5-(4-chloro-benzoyl)-2,3,4,5-tetrahydro-1<i>H</i>-pyrido[4,3-<i>b</i>]indole-8-sulfonic acid [ No CAS ]
  • 3
  • [ 24686-78-0 ]
  • [ 14002-51-8 ]
  • [ 98-71-5 ]
  • 2-benzoyl-5-(biphenyl-4-carbonyl)-2,3,4,5-tetrahydro-1<i>H</i>-pyrido[4,3-<i>b</i>]indole-8-sulfonic acid [ No CAS ]
  • 4
  • [ 98-71-5 ]
  • [ 1218-69-5 ]
  • 4-[3,5-bis(2-hydroxyphenyl)-1H-1,2,4-triazol-1-yl]benzenesulfonic acid [ No CAS ]
  • 5
  • [ 720-94-5 ]
  • [ 98-71-5 ]
  • [ 921617-76-7 ]
YieldReaction ConditionsOperation in experiment
82% With hydrogenchloride; In ethanol; water; at 20℃; for 8h;Heating / reflux; To a stirred suspension of p-hydrazino-benzenesulfonic acid (42 g, 0.223 mol) in ethanol (450 ml) 6N hydrochloric acid (74 ml, 0.446 mol) was added at room temperature, followed by addition of 4,4,4-trifluoro-l-(4-methyl-phenyl)-butane-l,3- dione (51.45 g, 0.223 mol). The obtained suspension was refluxed for 8 h, then concentrated in vacuo. The residue was dissolved in water (300 ml) and extracted with ethyl acetate (2 x 200 ml). The combined organic layers were washed with water (1 x 100 ml) and brine (1 x 100 ml), dried over MgSO4, decolorized, filtered and concentrated in vacuo. The obtained crystalline product was recrystallized from diisopropyl ether (300 ml) to yield 70.12 g (82 percent) of the title compound.
  • 6
  • [ 99183-34-3 ]
  • [ 98-71-5 ]
  • [ 1072069-89-6 ]
YieldReaction ConditionsOperation in experiment
83% Example 8. Preparation of 2,3-dimethyl-3-(4-carboxybutyl)-5-sulfoindolenyne, potassium salt (compound 8) A mixture of phenylhydrazine-p-sulphonic acid (compound 7) (1.8 g; 9.7 mmole), 6-methyl-7-oxooctane acid (compound 5) (2.0 g; 11.6 mmole), and glacial acetic acid (15 mL) was refluxed under stirring for 8 h, then an additional amount of acetic acid was added and treated with activated carbon. The solvent was removed and the residue was dissolved in methanol (10 mL). To solution obtained, there are added dropwise the solution of potassium hydroxide (600 mg; 10,56 mmole) in methanol (7 mL), isopropyl alcohol (15 mL), and diethyl ether (2 mL). The precipitate formed was collected by filtration and dried in vacuum desiccator over P2O5. 2,3-Dimethyl-3-(4-carboxybutyl)-5-sulfoindolenyne, potassium salt (compound 8) was obtained with yield of 3.47 g (83%), λmax 258 nm. Mass-spectrum (MALDI) (C15H19NO5S): found m/z 327.2, calculated m/z 325.38. 1H-NMR (D2O), δ (ppm): 0.45-0.7 (2H, m, CH2CH2CH2CH2COOH); 1.31 (3H, s, 3-CH3); 1.36 (2H, m, CH2CH2CH2CH2COOH); 1.88-2.14 (4H, m, CH2CH2CH2CH2COOH); 7.53 (1H, d, ArH), 7.8 (2H, m, ArH)
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