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[ CAS No. 38256-93-8 ] {[proInfo.proName]}

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Chemical Structure| 38256-93-8
Chemical Structure| 38256-93-8
Structure of 38256-93-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 38256-93-8 ]

CAS No. :38256-93-8 MDL No. :MFCD00144829
Formula : C4H11NO Boiling Point : -
Linear Structure Formula :CH3NHCH2CH2OCH3 InChI Key :KOHBEDRJXKOYHL-UHFFFAOYSA-N
M.W : 89.14 Pubchem ID :300977
Synonyms :

Calculated chemistry of [ 38256-93-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 6
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 25.23
TPSA : 21.26 ?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) : -7.09 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.72
Log Po/w (XLOGP3) : -0.35
Log Po/w (WLOGP) : -0.15
Log Po/w (MLOGP) : -0.18
Log Po/w (SILICOS-IT) : -0.04
Consensus Log Po/w : 0.2

Druglikeness

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

Water Solubility

Log S (ESOL) : 0.03
Solubility : 94.6 mg/ml ; 1.06 mol/l
Class : Highly soluble
Log S (Ali) : 0.37
Solubility : 207.0 mg/ml ; 2.32 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -1.16
Solubility : 6.21 mg/ml ; 0.0697 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 38256-93-8 ]

Signal Word:Danger Class:3,8
Precautionary Statements:P501-P240-P210-P233-P243-P241-P242-P264-P280-P370+P378-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338-P310-P403+P235-P405 UN#:2924
Hazard Statements:H314-H225 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 38256-93-8 ]

* 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 [ 38256-93-8 ]

[ 38256-93-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 38256-93-8 ]
  • [ 132898-96-5 ]
  • 2,3-dioxo-2,3-dihydro-1<i>H</i>-indole-5-sulfonic acid (2-methoxy-ethyl)-methyl-amide [ No CAS ]
  • 2
  • [ 4565-31-5 ]
  • [ 38256-93-8 ]
  • 5-formylthiophene-2-carboxylic acid N-(2-methoxyethyl)methylamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example 1-7 Synthesis of the present aldehyde derivative [Compound No. (o)] To a solution of 400 mg of 5-formylthiophene-2-carboxylic acid in dimethylformamide were added 540 mg of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride and 410 mul of triethylamine, and the mixture was stirred for 30 minutes under ice-cooling. To this reaction solution was added 300 mul of N-(2-methoxyethyl)methylamine, and the mixture was stirred at room temperature. After 10percent hydrochloric acid was added thereto, the mixture was extracted with ethyl acetate. An organic layer was washed with an aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate, and concentrated under reduced under reduced pressure. The resulting residue was washed with ethyl acetate to obtain 221 mg of 5-formylthiophene-2-carboxylic acid N-(2-methoxyethyl)methylamide [Compound No. (o)]. 1H-NMR (300MHz, CDCl3) delta (ppm): 3.22 (broad s, 3H), 3.42 (s, 3H), 3.55~3.75 (4H), 7.45 (d, 1H, J=3.6Hz), 7.69 (d, 1H, J=3.9Hz), 9.95 (s, 1H).
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