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[ CAS No. 102-49-8 ] {[proInfo.proName]}

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Chemical Structure| 102-49-8
Chemical Structure| 102-49-8
Structure of 102-49-8 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 102-49-8 ]

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Product Details of [ 102-49-8 ]

CAS No. :102-49-8 MDL No. :MFCD00008114
Formula : C7H7Cl2N Boiling Point : -
Linear Structure Formula :- InChI Key :IXHNFOOSLAWRBQ-UHFFFAOYSA-N
M.W : 176.04 Pubchem ID :1608
Synonyms :

Calculated chemistry of [ 102-49-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 44.14
TPSA : 26.02 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.61 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.92
Log Po/w (XLOGP3) : 2.48
Log Po/w (WLOGP) : 2.3
Log Po/w (MLOGP) : 2.72
Log Po/w (SILICOS-IT) : 2.72
Consensus Log Po/w : 2.43

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.87
Solubility : 0.236 mg/ml ; 0.00134 mol/l
Class : Soluble
Log S (Ali) : -2.67
Solubility : 0.375 mg/ml ; 0.00213 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.67
Solubility : 0.0375 mg/ml ; 0.000213 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.17

Safety of [ 102-49-8 ]

Signal Word:Danger Class:8
Precautionary Statements:P501-P264-P280-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P405 UN#:2735
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 102-49-8 ]

* 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 [ 102-49-8 ]

[ 102-49-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 3034-48-8 ]
  • [ 102-49-8 ]
  • [ 50591-77-0 ]
  • 2
  • [ 31872-62-5 ]
  • [ 102-49-8 ]
  • N-[(3,4-dichlorophenyl)methyl]-3-nitropyridin-4-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
57% In isopropyl alcohol;Reflux; <strong>[31872-62-5]4-Methoxy-3-nitropyridine</strong> (5.4g, 35mmoles) was suspended in isopropanol (30ml) and 3,4-dichlorbenzylamine (9.25g, 53mmoles) was added in isopropanol (10ml). Heated to reflux overnight. Allowed to cool to room temperature and filtered off the pale yellow solid. Washed with isopropanol and dried in a desiccator (8.9g). Took up in DCM (80ml), filtered and evaporated to give product as a yellow solid. (5.9g, 57%) (0572) [00293] 1H NMR (CDCh ppm) d 9.3 (s, 1 H0, 8.6 (m, 1 H), 8.3 (d, 1 H, J = 6 Hz), 7.5 (d, 1 H, J = 9 Hz), 7.45 (d, 1 H, J = 2.5 Hz), 7.2 (d of d, 1 H, J = 2, 9 Hz), 6.65 (d, 1 H, J = 6 Hz), 4.55 (d, 1 H, J = 6 Hz)
  • 3
  • [ 102-49-8 ]
  • [ 53554-29-3 ]
  • C14H13Cl2N3O3 [ No CAS ]
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