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[ CAS No. 7335-06-0 ] {[proInfo.proName]}

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Chemical Structure| 7335-06-0
Chemical Structure| 7335-06-0
Structure of 7335-06-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 7335-06-0 ]

CAS No. :7335-06-0 MDL No. :MFCD01632186
Formula : C6H13N Boiling Point : -
Linear Structure Formula :- InChI Key :ONQBOTKLCMXPOF-UHFFFAOYSA-N
M.W : 99.17 Pubchem ID :81782
Synonyms :

Calculated chemistry of [ 7335-06-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 35.65
TPSA : 3.24 ?2

Pharmacokinetics

GI absorption : Low
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) : -5.92 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.09
Log Po/w (XLOGP3) : 1.39
Log Po/w (WLOGP) : 0.72
Log Po/w (MLOGP) : 1.14
Log Po/w (SILICOS-IT) : 1.45
Consensus Log Po/w : 1.36

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.26
Solubility : 5.39 mg/ml ; 0.0544 mol/l
Class : Very soluble
Log S (Ali) : -1.06
Solubility : 8.61 mg/ml ; 0.0868 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.04
Solubility : 9.11 mg/ml ; 0.0918 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 7335-06-0 ]

Signal Word:Danger Class:3,8
Precautionary Statements:P210-P280-P305+P351+P338-P310 UN#:2733
Hazard Statements:H225-H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 7335-06-0 ]

* 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 [ 7335-06-0 ]

[ 7335-06-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7335-06-0 ]
  • [ 79477-87-5 ]
  • C13H12FNO [ No CAS ]
YieldReaction ConditionsOperation in experiment
4 g With di-tert-butyl peroxide; copper(ll) bromide; In acetonitrile; at 60℃; under 760.051 Torr; for 24h; 1 g (0.5 mmol, 50 mg), 2 g (0.6 mmol, 101 mg), acetonitrile (3 mL), copper bromide (0.05 mmol, 11 mg) and di-tert-butyl peroxide (1 mmol, 183 μL) were sequentially added to the reaction tube. The reaction was stirred at 60 C for 24 h under an air (1 atm) atmosphere. The reaction was then quenched with EtOAc (EtOAc) (EtOAc) Filtration, spin-drying, and silica gel column separation (petrole ether / ethyl acetate = 5 / 1) gave 4 g of the desired product
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