99.0% (GC)| A1455242|Formula:C8H16O2|Molecular Weight:144.211450000+ products instock " />

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[ CAS No. 149-57-5 ] {[proInfo.proName]}

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Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 149-57-5
Chemical Structure| 149-57-5
Structure of 149-57-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 149-57-5 ]

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Product Details of [ 149-57-5 ]

CAS No. :149-57-5 MDL No. :MFCD00002675
Formula : C8H16O2 Boiling Point : -
Linear Structure Formula :HOOCCH(C2H5)(CH2)3CH3 InChI Key :-
M.W : 144.21 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 149-57-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.88
Num. rotatable bonds : 5
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 42.34
TPSA : 37.3 ?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) : -5.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.93
Log Po/w (XLOGP3) : 2.64
Log Po/w (WLOGP) : 2.29
Log Po/w (MLOGP) : 1.96
Log Po/w (SILICOS-IT) : 1.6
Consensus Log Po/w : 2.08

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.07
Solubility : 1.24 mg/ml ; 0.00856 mol/l
Class : Soluble
Log S (Ali) : -3.07
Solubility : 0.122 mg/ml ; 0.000843 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.67
Solubility : 3.07 mg/ml ; 0.0213 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.92

Safety of [ 149-57-5 ]

Signal Word:Danger Class:8
Precautionary Statements:P501-P273-P260-P270-P202-P201-P264-P280-P337+P313-P305+P351+P338-P308+P311-P362+P364-P303+P361+P353-P301+P330+P331-P304+P340+P310-P405 UN#:3265
Hazard Statements:H312-H303-H314-H319-H360-H371-H402 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 149-57-5 ]

* 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 [ 149-57-5 ]

[ 149-57-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 78385-26-9 ]
  • [ 149-57-5 ]
  • C13H25BrO3 [ No CAS ]
  • 2
  • [ 937-14-4 ]
  • [ 73590-85-9 ]
  • [ 149-57-5 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; EXAMPLE 29 OMEPRAZOL A solution of 25 ml ethyl acetate and 1.7 ml (0.0103 mole) of 2-ethylhexanoic acid was prepared, to which there were added 4 g (0.0117 mole) of 96percent pure 5-methoxy-2-((3,5-dimethyl-4-methoxy-2-pyridinyl)methylthio)-1 H -benzimidazole, 3.06 g (0.01214 mole) of metachloroperbenzoic acid were added to the resulting solution over 23 minutes at temperatures of -35 and -40°C. When the addition was completed, the system was held -35°C for 1 hour. Thereafter, 1.8 ml of triethylamine (0.013 mole) was added at that temperature after which the temperature was held at-35°C for 20 minutes. The mixture was filtered at that temperature and washed with cold ethyl acetate at a temperature of -20°C. It was allowed to dry under flowing air at room temperature. A white solid (3.7 g) was obtained, representing a 94percent yield. The melting point of the product was 147-150°C.
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