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[ CAS No. 3621-81-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 3621-81-6
Chemical Structure| 3621-81-6
Structure of 3621-81-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 3621-81-6 ]

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Product Details of [ 3621-81-6 ]

CAS No. :3621-81-6 MDL No. :MFCD09264312
Formula : C7H3Cl2NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :JOXBFDPBVQGJOJ-UHFFFAOYSA-N
M.W : 188.01 Pubchem ID :10397578
Synonyms :

Calculated chemistry of [ 3621-81-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 44.03
TPSA : 26.03 ?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) : -4.77 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.35
Log Po/w (XLOGP3) : 3.77
Log Po/w (WLOGP) : 3.13
Log Po/w (MLOGP) : 2.17
Log Po/w (SILICOS-IT) : 3.18
Consensus Log Po/w : 2.92

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.99
Solubility : 0.0194 mg/ml ; 0.000103 mol/l
Class : Soluble
Log S (Ali) : -4.01
Solubility : 0.0184 mg/ml ; 0.0000977 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.15
Solubility : 0.0134 mg/ml ; 0.0000711 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.2

Safety of [ 3621-81-6 ]

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

Application In Synthesis of [ 3621-81-6 ]

* 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 [ 3621-81-6 ]

[ 3621-81-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 3621-81-6 ]
  • [ 287114-25-4 ]
  • C19H24ClN3O3 [ No CAS ]
  • 2
  • [ 3621-81-6 ]
  • [ 159877-36-8 ]
  • tert-butyl 6-(5-chlorobenzo[d]oxazol-2-yl)octahydro-1H-pyrrolo[3,4-b]pyridine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
76% With triethylamine; In dichloromethane; at 20℃; for 1h; A solution of Compound 6g (226 mg, 1 mmol) and Compound 9 (224 mg, 1.2 mmol) and TEA (200 mg, 2 mmol) in DCM (10 ml) was stirred at r.t. for 1 hr. The reaction was concentrated and purified by silica gel chromatography (elutingwith petroleum ether/EtOAc=100:1~6:1) to give compound 7a (350 mg, yield: 76%). 1H NMR (400MHz, CHLOROFORM-d) delta= 7.31 (d, J=2.0 Hz, 1H), 7.15 (d, J=8.6 Hz,1H), 6.97 (dd, J=2.0, 8.4 Hz, 1H), 4.06 (d, J=10.6 Hz, 1H), 3.81 (t, J=8.9 Hz, 1H),3.72 (dd, J=5.7, 10.6 Hz, 1H), 3.60 - 3.46 (m, 2H), 2.78 (t, J=12.3 Hz, 1H), 2.31 (qd,J=5.8, 11.9 Hz, 1H), 1.85 (d, J=11.9 Hz, 1H), 1.77 - 1.65 (m, 2H), 1.49 (s, 9H), 1.38-1.35 (m, 2H)
  • 3
  • [ 3621-81-6 ]
  • [ 94050-90-5 ]
  • C16H12ClNO5 [ No CAS ]
YieldReaction ConditionsOperation in experiment
90.4% 18.2 g of compound A1 was dissolved in 100 mL of DMF, 40 g of anhydrous potassium carbonate was added thereto with stirring, and the temperature was raised to 80 C, and the reaction was stirred for 1 hour, and the temperature was lowered to room temperature.Then 18.8 g of compound A2 was added in portions,The reaction was continued to warm to 80 C and the reaction was stirred for 1 hour and allowed to cool to room temperature.Dilute with 500 mL of water, adjust the pH to about 3 with hydrochloric acid, and precipitate a large amount of white solid.Filter by suction. The filter cake was dried to give 30.1 g of a white solid, Compound A3.The yield was 90.4%, and the HPLC purity was greater than 95%.
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