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[ CAS No. 72080-83-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 72080-83-2
Chemical Structure| 72080-83-2
Structure of 72080-83-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 72080-83-2 ]

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Product Details of [ 72080-83-2 ]

CAS No. :72080-83-2 MDL No. :MFCD02094510
Formula : C10H14N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :QMMFTRJQCCVPCE-UHFFFAOYSA-N
M.W : 194.23 Pubchem ID :2794257
Synonyms :

Calculated chemistry of [ 72080-83-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.3
Num. rotatable bonds : 6
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 53.01
TPSA : 64.35 ?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) : -6.96 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.94
Log Po/w (XLOGP3) : 0.74
Log Po/w (WLOGP) : 0.72
Log Po/w (MLOGP) : 0.96
Log Po/w (SILICOS-IT) : 0.77
Consensus Log Po/w : 1.03

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.43
Solubility : 7.19 mg/ml ; 0.037 mol/l
Class : Very soluble
Log S (Ali) : -1.67
Solubility : 4.15 mg/ml ; 0.0214 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.0
Solubility : 0.196 mg/ml ; 0.00101 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.99

Safety of [ 72080-83-2 ]

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 [ 72080-83-2 ]

* 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 [ 72080-83-2 ]

[ 72080-83-2 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 5430-45-5 ]
  • [ 72080-83-2 ]
  • N-(2-benzyloxycarbonylaminoethyl)-5-chloroisoquinoline-8-sulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In methanol; chlorosulfonic acid; chloroform; (1) A solution of 5.00 g of <strong>[5430-45-5]5-chloroisoquinoline</strong> in 8ml of chlorosulfonic acid was heated for 3 hours at 170 C. After cooling, the reaction mixture was poured into ice-water and extracted with chloroform. The chloroform layer was washed with water, dried and then added to a solution of 5.87 g of 2-(N-benzyloxycarbonylamino)ethylamine and 10 ml of triethylamine in 50 ml of methanol under ice-water cooling with stirring. The reaction mixture was stirred for 2 hours at room temperature and then filtered. The filtrate was concentrated and to the residue was added chloroform. The obtained precipitate was filtered off to give 2.50 g of N-(2-benzyloxycarbonylaminoethyl)-<strong>[5430-45-5]5-chloroisoquinoline</strong>-8-sulfonamide as colorless crystals.
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