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[ CAS No. 97-08-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 97-08-5
Chemical Structure| 97-08-5
Structure of 97-08-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 97-08-5 ]

CAS No. :97-08-5 MDL No. :MFCD00007440
Formula : C6 H3 Cl2 N O4 S Boiling Point : -
Linear Structure Formula :- InChI Key :SEWNAJIUKSTYOP-UHFFFAOYSA-N
M.W : 256.06 Pubchem ID :7323
Synonyms :

Calculated chemistry of [ 97-08-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 53.36
TPSA : 88.34 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.36 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.08
Log Po/w (XLOGP3) : 2.12
Log Po/w (WLOGP) : 3.26
Log Po/w (MLOGP) : 1.03
Log Po/w (SILICOS-IT) : -0.06
Consensus Log Po/w : 1.48

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.95
Solubility : 0.288 mg/ml ; 0.00113 mol/l
Class : Soluble
Log S (Ali) : -3.61
Solubility : 0.0634 mg/ml ; 0.000248 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.94
Solubility : 0.295 mg/ml ; 0.00115 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.21

Safety of [ 97-08-5 ]

Signal Word:Danger Class:8
Precautionary Statements:P260-P280-P303+P361+P353-P301+P330+P331-P304+P340+P310-P305+P351+P338+P310 UN#:3261
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 97-08-5 ]

* 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 [ 97-08-5 ]

[ 97-08-5 ] Synthesis Path-Downstream   1~16

  • 1
  • [ 110-89-4 ]
  • [ 97-08-5 ]
  • [ 53162-43-9 ]
  • 2
  • [ 97-08-5 ]
  • 4-Amino-1-hydroxy-N-[4-(2,4-di-tert-pentylphenoxy)butyl]-2-naphthamide [ No CAS ]
  • [ 58596-13-7 ]
  • 3
  • [ 97-08-5 ]
  • [ 13518-40-6 ]
  • [ 873923-16-1 ]
  • 4
  • [ 97-08-5 ]
  • [ 20781-23-1 ]
  • [ 921195-72-4 ]
  • 5
  • [ 97-08-5 ]
  • [ 160232-08-6 ]
  • [ 854746-19-3 ]
  • 6
  • [ 769169-26-8 ]
  • [ 97-08-5 ]
  • 4-Chloro-3-nitro-N-(3,3,3-trifluoro-1-hydroxymethyl-2-trifluoromethyl-propyl)-benzenesulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
13% With triethylamine; In dichloromethane; at 0 - 25℃; for 16.25h; Example 5 4-Chloro-3-nitro-N-(3,3,3-trifluoro-1-hydroxymethyl-2-trifluoromethyl-propyl)-benzenesulfonamide To a solution of 4,4,4,4',4',4'-hexafluoro-dl-valinol (0.50 g, 2.37 mmol), triethylamine (0.43 mL, 3.08 mmol) and CH2Cl2 (17.5 mL) at 0 C. was added a previously dissolved mixture of 4-chloro-3-nitro-benzenesulfonyl chloride (0.606 g, 2.37 mmol) in CH2Cl2 (5 mL). After 15 min, the ice bath was removed and the reaction allowed to warm up to 25 C. After 16 h, the reaction was then diluted with CH2Cl2 (20 mL) and poured into a separatory funnel containing a saturated NaHCO3 solution. The organic phase was separated, washed sequentially with 1N HCl solution, distilled water, brine, dried over MgSO4 and evaporated to afford the crude product which was purified using Biotage Flash chromatography, eluent: 3:1 hexanes-ethyl acetate, to afford the product as a solid (0.134 g, 13%). MS (-ESI) 428.9 ([M-H]-).
  • 13
  • [ 97-08-5 ]
  • <i>N</i>,<i>N</i>-bis-(2,4-dimethoxy-benzyl)-4-(1-methyl-3-phenyl-ureido)-3-nitro-benzenesulfonamide [ No CAS ]
  • 14
  • [ 97-08-5 ]
  • <i>N</i>,<i>N</i>-bis-(2,4-dimethoxy-benzyl)-4-(1,3-dimethyl-3-phenyl-ureido)-3-nitro-benzenesulfonamide [ No CAS ]
  • 16
  • [ 97-08-5 ]
  • N-{4-[4-(3,3-diphenyl-allyl)-piperazin-1-yl]-benzoyl}-4-(1-methyl-3-phenylureido)-3-nitro-benzenesulfonamide [ No CAS ]
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