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[ CAS No. 5744-68-3 ]

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Chemical Structure| 5744-68-3
Chemical Structure| 5744-68-3
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Product Details of [ 5744-68-3 ]

CAS No. :5744-68-3 MDL No. :MFCD00233969
Formula : C4H5BrN2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W :161.00 g/mol Pubchem ID :-
Synonyms :

Calculated chemistry of [ 5744-68-3 ]

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.25
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 31.25
TPSA : 28.68 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.12 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.08
Log Po/w (XLOGP3) : 1.64
Log Po/w (WLOGP) : 1.48
Log Po/w (MLOGP) : 0.81
Log Po/w (SILICOS-IT) : 2.18
Consensus Log Po/w : 1.44

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.4
Solubility : 0.641 mg/ml ; 0.00398 mol/l
Class : Soluble
Log S (Ali) : -1.86
Solubility : 2.25 mg/ml ; 0.014 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.46
Solubility : 0.554 mg/ml ; 0.00344 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.76

Safety of [ 5744-68-3 ]

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

Application In Synthesis of [ 5744-68-3 ]

* 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 [ 5744-68-3 ]

[ 5744-68-3 ] Synthesis Path-Downstream   1~6

  • 3
  • {{(C5Me5)Rh}2(μ-OH)3}BF4 [ No CAS ]
  • [ 5744-68-3 ]
  • [ 829-85-6 ]
  • {{(C5Me5)Rh}2(μ-bmpz)(μ-OH)(μ-PPh2)}BF4 [ No CAS ]
  • {{(C5Me5)Rh}2(μ-bmpz)(μ-PPh2)2}BF4 [ No CAS ]
  • 4
  • {(Rh(C5(CH3)5))2(OH)3}(1+)*BF4(1-)={(Rh(C5(CH3)5))2(OH)3}(BF4) [ No CAS ]
  • [ 5744-68-3 ]
  • [ 829-85-6 ]
  • {(Rh(C5(CH3)5))2(NNC(Br)CHC(CH3))(Cl)(P(C6H5)2)}(1+)*BF4(1-)={(Rh(C5(CH3)5))2(NNC(Br)CHC(CH3))(Cl)(P(C6H5)2)}(BF4) [ No CAS ]
  • 5
  • [ 100-39-0 ]
  • [ 5744-68-3 ]
  • 1-benzyl-5-bromo-3-methyl-1H-pyrazole [ No CAS ]
  • 6
  • [ 591-50-4 ]
  • [ 5744-68-3 ]
  • [ 41327-15-5 ]
YieldReaction ConditionsOperation in experiment
87% (1) Preparation of Compound IIIa: Compound IV (160g, 1mol) was added to 900ml of tetrahydrofuran,Was slowly added portionwise sodium tert-butoxide (115.2g, 1.2mol), stirred for 20 minutes, a solution of iodine benzene (243.6g, 1.2mol). The mixture was heated at reflux for 4 hours with stirring, and then stirred at room temperature overnight, TLC showed the reaction was complete, the reaction mixture was slowly poured into ice water, ethyl acetate was added, the organic phase was separated, the aqueous phase was again extracted with ethyl acetate, the organic phases combined, dried and concentrated to give compound IIIa205.3g, a yield of 87percent.
With pyridine; In acetonitrile; Compound IV was run in acetonitrile, pyridine,With the compound iodobenzene nucleophilic substitution reaction preparation of compound III,
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