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[ CAS No. 4771-47-5 ] {[proInfo.proName]}

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Chemical Structure| 4771-47-5
Chemical Structure| 4771-47-5
Structure of 4771-47-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 4771-47-5 ]

CAS No. :4771-47-5 MDL No. :MFCD00007087
Formula : C7H4ClNO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :VCHSXYHBMFKRBK-UHFFFAOYSA-N
M.W : 201.56 Pubchem ID :20902
Synonyms :

Calculated chemistry of [ 4771-47-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.23
TPSA : 83.12 ?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) : -6.17 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.79
Log Po/w (XLOGP3) : 1.91
Log Po/w (WLOGP) : 1.95
Log Po/w (MLOGP) : 1.11
Log Po/w (SILICOS-IT) : -0.26
Consensus Log Po/w : 1.1

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.5
Solubility : 0.634 mg/ml ; 0.00314 mol/l
Class : Soluble
Log S (Ali) : -3.28
Solubility : 0.106 mg/ml ; 0.000526 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.77
Solubility : 3.4 mg/ml ; 0.0169 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.74

Safety of [ 4771-47-5 ]

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

Application In Synthesis of [ 4771-47-5 ]

* 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.

  • Upstream synthesis route of [ 4771-47-5 ]
  • Downstream synthetic route of [ 4771-47-5 ]

[ 4771-47-5 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 4771-47-5 ]
  • [ 41252-95-3 ]
YieldReaction ConditionsOperation in experiment
96% With copper(I) oxide; potassium phosphate; bismuth (III) nitrate pentahydrate; palladium(II) trifluoroacetate; oxygen; sodium iodide In dimethyl sulfoxide at 170℃; for 20 h; Schlenk technique In a Schlenk reaction tube equipped with a magnetic stirrer, 6.7 mg of palladium trifluoroacetate was added.Cuprous oxide 28.6mg,Potassium phosphate 6.4mg,4,5-Difluoro-2-nitrobenzoic acid 40.3mg,Sodium iodide 36mg,Bismuth nitrate pentahydrate 194 mg and 2 mL of dimethyl sulfoxide.The reaction was heated at 170°C for 20 hours in the presence of oxygen. After the reaction is completed, distilled water is added to quench the reaction.Extraction with ethyl acetate 3 times each 10 mL, the combined organic phases were concentrated to give 1-chloro-4-iodo-2-nitrobenzene54.4 mg, 96percent yield
Reference: [1] Patent: CN107513020, 2017, A, . Location in patent: Paragraph 0066-0067
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