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[ CAS No. 51857-17-1 ] {[proInfo.proName]}

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Chemical Structure| 51857-17-1
Chemical Structure| 51857-17-1
Structure of 51857-17-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 51857-17-1 ]

CAS No. :51857-17-1 MDL No. :MFCD00671489
Formula : C11H24N2O2 Boiling Point : -
Linear Structure Formula :C4H9OC(O)NH(CH2)6NH2 InChI Key :RVZPDKXEHIRFPM-UHFFFAOYSA-N
M.W : 216.32 Pubchem ID :2733170
Synonyms :
Chemical Name :N-Boc-1,6-Diaminohexane

Calculated chemistry of [ 51857-17-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.91
Num. rotatable bonds : 9
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 62.21
TPSA : 64.35 ?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) : -6.61 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.67
Log Po/w (XLOGP3) : 1.42
Log Po/w (WLOGP) : 2.03
Log Po/w (MLOGP) : 1.55
Log Po/w (SILICOS-IT) : 1.39
Consensus Log Po/w : 1.81

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.48
Solubility : 7.13 mg/ml ; 0.033 mol/l
Class : Very soluble
Log S (Ali) : -2.38
Solubility : 0.91 mg/ml ; 0.00421 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.91
Solubility : 0.267 mg/ml ; 0.00124 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.23

Safety of [ 51857-17-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313 UN#:N/A
Hazard Statements:H315-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 51857-17-1 ]

* 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 [ 51857-17-1 ]

[ 51857-17-1 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 51857-17-1 ]
  • [ 72040-63-2 ]
  • (6-{6-[5-(2-oxo-hexahydro-thieno[3,4-d]imidazol-4-yl)-pentanoylamino]-hexanoylamino}-hexyl)-carbamic acid tert-butyl ester [ No CAS ]
  • 2
  • [ 51857-17-1 ]
  • [ 7310-97-6 ]
  • [ 1448695-79-1 ]
  • 3
  • [ 51857-17-1 ]
  • [ 169624-67-3 ]
  • C37H45N3O7 [ No CAS ]
YieldReaction ConditionsOperation in experiment
0.9 g Synthesis of Fmoc-Phe-Gly-NH-(CH2)6NH-Boc To a solution of <strong>[169624-67-3]Fmoc-Phe-Gly-OH</strong> (0.66 g) in anhydrous THF (20 mL) at 0 C. under N2 was added N,N'-dicyclohexylcarbodiimide (0.307 g) and 1-hydroxybenzotriazole hydrate (0.201 g). After stirring for 15 min, N-Boc-1,6-diaminohexane (0.322 g) was added. The reaction mixture was allowed to warm to RT and stirred overnight. Solids were filtered off and they were washed with EtOAc. The filtrate and washings were then concentrated under reduced pressure. The resulting residue was purified by flash column chromatography (0 to 10% MeOH in CH2Cl2) to afford Fmoc-Phe-Gly-NH-(CH2)6NH-Boc as a white solid (0.9 g).
  • 4
  • [ 55750-49-7 ]
  • [ 51857-17-1 ]
  • [ 124529-64-2 ]
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