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[ CAS No. 112898-23-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 112898-23-4
Chemical Structure| 112898-23-4
Structure of 112898-23-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 112898-23-4 ]

CAS No. :112898-23-4 MDL No. :MFCD00070261
Formula : C23H44N2O4S Boiling Point : -
Linear Structure Formula :- InChI Key :FJACYLCGMGYDOE-HMZWWLAASA-N
M.W : 444.67 Pubchem ID :56777359
Synonyms :

Calculated chemistry of [ 112898-23-4 ]

Physicochemical Properties

Num. heavy atoms : 30
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.91
Num. rotatable bonds : 9
Num. H-bond acceptors : 5.0
Num. H-bond donors : 3.0
Molar Refractivity : 127.28
TPSA : 112.96 Ų

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.72
Log Po/w (XLOGP3) : 2.96
Log Po/w (WLOGP) : 5.35
Log Po/w (MLOGP) : 3.14
Log Po/w (SILICOS-IT) : 0.91
Consensus Log Po/w : 3.21

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.87
Solubility : 0.0603 mg/ml ; 0.000136 mol/l
Class : Soluble
Log S (Ali) : -4.99
Solubility : 0.0045 mg/ml ; 0.0000101 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -1.58
Solubility : 11.8 mg/ml ; 0.0265 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 4.58

Safety of [ 112898-23-4 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 112898-23-4 ]

* 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 [ 112898-23-4 ]

[ 112898-23-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 112898-23-4 ]
  • [ 112898-22-3 ]
YieldReaction ConditionsOperation in experiment
98% With hydrogenchloride In water 3A.1 Stepl:An aqueous solution of the dicyclohexylamine salt of compound 3a1 (0.5 g, 1.12mmol) was adjusted to pH 2 by addition of 1M HCI and the resulting aqueous phasewas extracted twice with EtOAc. The EtOAc phase was dried (MgSO4), filtered andconcentrated) to give 290 mg (1.10 mmol, 98%) of the free acid. The free acid wasdissolved in 4M HCI/dioxane (5 ml_) and the mixture was stirred at room temperaturefor 1 hour. The solvent was evaporated and the residue 3a2 was dried under vacuumand used as is in the next step.
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