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[ CAS No. 5041-09-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 5041-09-8
Chemical Structure| 5041-09-8
Structure of 5041-09-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 5041-09-8 ]

CAS No. :5041-09-8 MDL No. :MFCD00060199
Formula : C4H12ClN Boiling Point : No data available
Linear Structure Formula :- InChI Key :BSMNBEHEFWDHJD-UHFFFAOYSA-N
M.W : 109.60 Pubchem ID :12206183
Synonyms :

Calculated chemistry of [ 5041-09-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 6
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 31.01
TPSA : 26.02 ?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) : -5.88 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.53
Log Po/w (WLOGP) : 1.4
Log Po/w (MLOGP) : 1.16
Log Po/w (SILICOS-IT) : 0.03
Consensus Log Po/w : 0.82

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 3.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.42
Solubility : 4.19 mg/ml ; 0.0382 mol/l
Class : Very soluble
Log S (Ali) : -1.69
Solubility : 2.26 mg/ml ; 0.0206 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.61
Solubility : 26.8 mg/ml ; 0.244 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 5041-09-8 ]

Signal Word:Warning Class:
Precautionary Statements:P305+P351+P338 UN#:
Hazard Statements:H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 5041-09-8 ]

* 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 [ 5041-09-8 ]

[ 5041-09-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 96-26-4 ]
  • [ 5041-09-8 ]
  • [ 226930-88-7 ]
  • [ 38993-84-9 ]
YieldReaction ConditionsOperation in experiment
45% 33-1) 5-Hydroxymethyl-1-isobutylimidazole The title compound was obtained in a yield of 45percent according to the same procedure as Preparation 31-1) using dihydroxyacetone and isobutylamine hydrochloride as starting materials. 1H NMR(CDCl3) delta0.90(d, 6H), 1.76(m, 1H), 3.62(d, 2H), 4.24(brs, 1H), 4.60(s, 2H), 6.85(s, 1H), 7.45(s, 1H)
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