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[ CAS No. 1458-03-3 ] {[proInfo.proName]}

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Chemical Structure| 1458-03-3
Chemical Structure| 1458-03-3
Structure of 1458-03-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1458-03-3 ]

CAS No. :1458-03-3 MDL No. :MFCD00834965
Formula : C6H6ClN3O2 Boiling Point : -
Linear Structure Formula :- InChI Key :JGAJCAJHSHUPGH-UHFFFAOYSA-N
M.W : 187.58 Pubchem ID :824637
Synonyms :

Calculated chemistry of [ 1458-03-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.17
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 42.73
TPSA : 78.1 ?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) : -6.64 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.21
Log Po/w (XLOGP3) : 1.13
Log Po/w (WLOGP) : 0.51
Log Po/w (MLOGP) : -0.41
Log Po/w (SILICOS-IT) : 0.69
Consensus Log Po/w : 0.62

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.95
Solubility : 2.09 mg/ml ; 0.0111 mol/l
Class : Very soluble
Log S (Ali) : -2.36
Solubility : 0.812 mg/ml ; 0.00433 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.99
Solubility : 1.93 mg/ml ; 0.0103 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.14

Safety of [ 1458-03-3 ]

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 [ 1458-03-3 ]

* 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 [ 1458-03-3 ]

[ 1458-03-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1458-03-3 ]
  • [ 13457-28-8 ]
YieldReaction ConditionsOperation in experiment
87% Into a 500 ml three-necked flask, 100 mL of acetic acid was added, and Compound 2 (20 g, 0.11 mol) was added dropwise to a 100 mL aqueous solution of 40% hydrogen bromide at 0C. The reaction was completed after 30 minutes of dropwise addition. A 50 ml aqueous solution of sodium nitrite (20.7 g, 0.33 mol) was added dropwise at a controlled temperature of 0C. After 30 minutes of reaction, the reaction is complete and it is quenched by the dropwise addition of 30 ml of 10% sodium bisulfite solution. Ethyl acetate extraction (200ml×2), dried over 20g of anhydrous sodium sulfate, The mixture was concentrated by suction filtration to obtain a white solid compound 3 (23.3 g, yield 87%).
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