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[ CAS No. 1501-26-4 ] {[proInfo.proName]}

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Chemical Structure| 1501-26-4
Chemical Structure| 1501-26-4
Structure of 1501-26-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1501-26-4 ]

CAS No. :1501-26-4 MDL No. :MFCD00000756
Formula : C6H9ClO3 Boiling Point : -
Linear Structure Formula :ClCO(CH2)3COOCH3 InChI Key :JCAZSWWHFJVFPP-UHFFFAOYSA-N
M.W : 164.59 Pubchem ID :73916
Synonyms :

Calculated chemistry of [ 1501-26-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.67
Num. rotatable bonds : 5
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 37.24
TPSA : 43.37 ?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) : -6.4 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.85
Log Po/w (XLOGP3) : 1.28
Log Po/w (WLOGP) : 1.1
Log Po/w (MLOGP) : 0.64
Log Po/w (SILICOS-IT) : 1.35
Consensus Log Po/w : 1.24

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.34
Solubility : 7.58 mg/ml ; 0.046 mol/l
Class : Very soluble
Log S (Ali) : -1.79
Solubility : 2.67 mg/ml ; 0.0162 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.73
Solubility : 3.09 mg/ml ; 0.0187 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.67

Safety of [ 1501-26-4 ]

Signal Word:Danger Class:8
Precautionary Statements:P260-P261-P264-P270-P271-P280-P301+P312-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P310-P312-P321-P322-P330-P363-P405-P501 UN#:3265
Hazard Statements:H302-H312-H314-H332 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1501-26-4 ]

* 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 [ 1501-26-4 ]

[ 1501-26-4 ] Synthesis Path-Downstream   1~6

  • 2
  • [ 1501-26-4 ]
  • [ 5713-61-1 ]
  • [ 18760-47-9 ]
  • 3
  • [ 1501-26-4 ]
  • [ 6574-15-8 ]
  • 4
  • [ 51792-34-8 ]
  • [ 1501-26-4 ]
  • [ 1209418-96-1 ]
  • 5
  • [ 25560-00-3 ]
  • [ 207399-07-3 ]
  • [ 1501-26-4 ]
  • [ 1313374-54-7 ]
YieldReaction ConditionsOperation in experiment
1 (300 mg, 0.45 mmol, 1 equiv) and l-(3-aminopropyl)-2-pipecoline (170 mg, 0.9 mmol, 2 equiv) were dissolved in ACN (2 mL), and DIEA (87 iL, 0.67 mmol, 1.5 equiv) was added. The reaction mixture was heated at 80 C for 40 minutes, and the resulting blue mixture was neutralized with 0.1 N HCl and concentrated under vacuum. The blue mixture was dissolved in DCM under N2 atmosphere, and treated with excess DIEA (700 iL, 5.39 mmol, 12 equiv) and methyl 4- (chloroformyl)butyrate (110 μ, 0.67 mmol, 1.5 equiv) at 0 C for 15 minutes. The resulting green product 2 was washed with 0.1 N HCl and brine, concentrated under vacuum, and used without further purification.
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