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[ CAS No. 2403-88-5 ] {[proInfo.proName]}

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Type HazMat fee for 500 gram (Estimated)
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Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 2403-88-5
Chemical Structure| 2403-88-5
Structure of 2403-88-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2403-88-5 ]

CAS No. :2403-88-5 MDL No. :MFCD00005983
Formula : C9H19NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :VDVUCLWJZJHFAV-UHFFFAOYSA-N
M.W : 157.25 Pubchem ID :75471
Synonyms :

Calculated chemistry of [ 2403-88-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 51.22
TPSA : 32.26 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.62 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.21
Log Po/w (XLOGP3) : 0.9
Log Po/w (WLOGP) : 0.91
Log Po/w (MLOGP) : 1.22
Log Po/w (SILICOS-IT) : 1.52
Consensus Log Po/w : 1.35

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.38
Solubility : 6.53 mg/ml ; 0.0415 mol/l
Class : Very soluble
Log S (Ali) : -1.16
Solubility : 10.8 mg/ml ; 0.0688 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.03
Solubility : 1.48 mg/ml ; 0.0094 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.41

Safety of [ 2403-88-5 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3259
Hazard Statements:H314-H317 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2403-88-5 ]

* 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 [ 2403-88-5 ]

[ 2403-88-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 2403-88-5 ]
  • [ 1202-25-1 ]
  • 1-(2,2,6,6-tetramethylpiperidine-4-yl)-4-(N,N-dimethylamino)benzoate [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 1 A mixture of 18 g of methyl p-dimethylaminobenzoate, 15.7 g of 2,2,6,6-tetramethyl-4-hydroxypiperidine and 0.2 ml tetrabutyl ortotitanate is heated and stirred for 6 hours at 170 C. The reaction product is recrystallized from petroleum ether at 100/120 C. and decolourized with decolourizing earth. 4-(p-dimethylamino-benzoyloxy)-2,2,6,6-tetramethylpiperidine is obtained in form of a crystalline white substance with m.p. 137-139 C. and specific extinction (E:)--992 at 312 nm.
EXAMPLE 1 A mixture of 18 g of methyl p-dimethylaminobenzoate, 15.7 g of 2,2,6,6-tetramethyl-4-hydroxypiperidine and 0.2 ml tetrabutyl ortotitanate is heated and stirred for 6 hours at 170C. The reaction product is recrystallized from petroleum ether at 100/120C and decolourized with decolourizing earth. 4-(p-dimethylamino-benzoyloxy)-2,2,6,6-tetramethylpiperidine is obtained in form of a crystalline white substance with m.p. 137-139C and specific extinction (E:) - 992 at 312 nm.
  • 2
  • [ 2403-88-5 ]
  • [ 327056-62-2 ]
  • C15H21N3O [ No CAS ]
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