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[ CAS No. 4521-33-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 4521-33-9
Chemical Structure| 4521-33-9
Structure of 4521-33-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 4521-33-9 ]

CAS No. :4521-33-9 MDL No. :MFCD00005433
Formula : C5H3NO3S Boiling Point : -
Linear Structure Formula :- InChI Key :CHTSWZNXEKOLPM-UHFFFAOYSA-N
M.W : 157.15 Pubchem ID :78281
Synonyms :

Calculated chemistry of [ 4521-33-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 38.53
TPSA : 91.13 ?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) : -6.15 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.72
Log Po/w (XLOGP3) : 1.56
Log Po/w (WLOGP) : 1.47
Log Po/w (MLOGP) : -0.82
Log Po/w (SILICOS-IT) : 0.57
Consensus Log Po/w : 0.7

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.04
Solubility : 1.45 mg/ml ; 0.00922 mol/l
Class : Soluble
Log S (Ali) : -3.08
Solubility : 0.13 mg/ml ; 0.000825 mol/l
Class : Soluble
Log S (SILICOS-IT) : -0.98
Solubility : 16.3 mg/ml ; 0.104 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.29

Safety of [ 4521-33-9 ]

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

Application In Synthesis of [ 4521-33-9 ]

* 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 [ 4521-33-9 ]

[ 4521-33-9 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 4521-33-9 ]
  • [ 6973-09-7 ]
  • 5-(5'-Nitro-2'-thienylmethylideneamino)-2-toluenesulfonamide [ No CAS ]
  • 2
  • [ 4521-33-9 ]
  • [ 17115-51-4 ]
  • [ 28566-12-3 ]
  • 2,3,4,5,6,8-hexahydro-8-(5-nitro-2-thienyl)-7H-cyclopenta[b]thieno[2,3-e]pyridin-7-one, 1,1-dioxide [ No CAS ]
  • 4
  • [ 4521-33-9 ]
  • [ 1986-47-6 ]
  • (1S*,2R*)-N-((5-nitrothiophen-2-yl)methyl)-2-phenylcyclopropan-1-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
40% General procedure: Trans-2-phenylcyclopropylamine hydrochloride (1.0 eq.), acetic acid (1.0eq.) and the appropriate aldehyde (0.9 eq.) were dissolved in around bottom flask in 10 mL dry DCE. The reaction mixture was stirred gently at room temperature for 2 h before sodium triacetoxyborohydride (3.0 eq.) was added in small portions to the reaction vessel. The reaction was monitored by TLC and quenched using 10 mL of an aqueous (5%) NaHCO3 solution. The organic layer was separated and the aqueous layer extracted three times with10 mL of DCE. All organic layers were combined, dried over anhydrous Na2SO4, concentrated in vacuo and purified using flash chromatography (silica gel; cyclohexane/ethyl acetate) to give the desired compound.
  • 5
  • [ 4521-33-9 ]
  • [ 15980-22-0 ]
  • (E)-2,6-dimethyl-4-(((5-nitrothiophen-2-yl)methylene)amino)phenol [ No CAS ]
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