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[ CAS No. 17407-55-5 ] {[proInfo.proName]}

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Chemical Structure| 17407-55-5
Chemical Structure| 17407-55-5
Structure of 17407-55-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 17407-55-5 ]

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Product Details of [ 17407-55-5 ]

CAS No. :17407-55-5 MDL No. :MFCD00066443
Formula : C5H10O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :NGEWQZIDQIYUNV-BYPYZUCNSA-N
M.W : 118.13 Pubchem ID :853180
Synonyms :

Calculated chemistry of [ 17407-55-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.8
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 29.08
TPSA : 57.53 ?2

Pharmacokinetics

GI absorption : High
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) : -6.67 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.97
Log Po/w (XLOGP3) : 0.5
Log Po/w (WLOGP) : 0.09
Log Po/w (MLOGP) : 0.01
Log Po/w (SILICOS-IT) : -0.3
Consensus Log Po/w : 0.25

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.76
Solubility : 20.7 mg/ml ; 0.176 mol/l
Class : Very soluble
Log S (Ali) : -1.28
Solubility : 6.23 mg/ml ; 0.0527 mol/l
Class : Very soluble
Log S (SILICOS-IT) : 0.5
Solubility : 374.0 mg/ml ; 3.17 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.46

Safety of [ 17407-55-5 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 17407-55-5 ]

* 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 [ 17407-55-5 ]

[ 17407-55-5 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 17407-55-5 ]
  • [ 13850-91-4 ]
  • (R)-2-(tert-Butoxycarbonyl-methyl-amino)-3-methyl-butyric acid (S)-1-carboxy-2-methyl-propyl ester [ No CAS ]
  • 2
  • [ 1342309-23-2 ]
  • [ 17407-56-6 ]
  • [ 17407-55-5 ]
  • [ 312-84-5 ]
  • [ 56-45-1 ]
  • [ 20312-37-2 ]
  • [ 13748-90-8 ]
  • [ 3060-46-6 ]
  • [ 63-91-2 ]
  • [ 31321-74-1 ]
  • [ 673-06-3 ]
  • 3
  • [ 1342309-24-3 ]
  • [ 17407-56-6 ]
  • [ 17407-55-5 ]
  • [ 312-84-5 ]
  • [ 56-45-1 ]
  • [ 20312-37-2 ]
  • [ 13748-90-8 ]
  • [ 3060-46-6 ]
  • [ 63-91-2 ]
  • [ 31321-74-1 ]
  • [ 673-06-3 ]
  • 4
  • Alloc-Me-Ala [ No CAS ]
  • N-Fmoc-N-methyl-L-threonine [ No CAS ]
  • 2-chlorotrityl chloride polystyrene resin [ No CAS ]
  • [ 17407-55-5 ]
  • [ 68858-20-8 ]
  • [ 35661-39-3 ]
  • (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-methoxypropanoic acid [ No CAS ]
  • [ 103478-62-2 ]
  • [ 143674-78-6 ]
  • [ 138775-22-1 ]
  • C62H103N10O16Pol [ No CAS ]
  • 5
  • Alloc-Me-Ala [ No CAS ]
  • N-Fmoc-N-methyl-L-threonine [ No CAS ]
  • [ 17407-55-5 ]
  • [ 68858-20-8 ]
  • [ 35661-39-3 ]
  • (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-methoxypropanoic acid [ No CAS ]
  • [ 103478-62-2 ]
  • [ 143674-78-6 ]
  • [ 138775-22-1 ]
  • C78H116N10O18 [ No CAS ]
  • 6
  • odobromoamide [ No CAS ]
  • [ 72-18-4 ]
  • [ 17407-55-5 ]
  • [ 2480-23-1 ]
  • [ 4125-98-8 ]
  • [ 147-85-3 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In water; at 105℃; for 12h; Absolute Configurations of Amino Acid Residues in 1.Odobromoamide (1, 1.2 mg) was treated with 5 M HCl (0.5mL) at 105 C for 12 h. The hydrolysate was concentrated todryness and partitioned between H2O and EtOAc. The aqueouslayer was subjected to HPLC [Cosmosil HILIC (4.6 250mm), MeCN/10 mM AcONH4 = 85:15 at 1.0 mL/min, UV detection at 215 nm] to yield N-Me-Ile, N-Me-Val, Hmba, Val andPro. Each amino acid expect for Hmba was added with 0.1%solution of Nα-(5-fluoro-2,4-dinitrophenyl)-L-alaninamide (LFDAA, Marfey’s reagent, 200 L) in acetone and 0.5 MNaHCO3 (100 L) followed by heating at 40 C for 90 min.After cooling to room temperature, the reaction mixture wasneutralized with 2 M HCl (25 L) and diluted with MeOH(300 L). The solution was subjected to reversed-phase HPLC[Cosmosil 5C18-AR-II (4.6 250 mm), MeOH/20 mM AcONa = 60:40 (solvent A) or 50:50 (solvent B) at 1.0 mL/min,UV detection at 340 nm]. The L-FDAA derivatives of standardamino acids were prepared by the same procedure. The retention times (min) of the authentic standards were as follows: LN-Me-Ile (6.6), L-allo-N-Me-Ile (6.9), D-N-Me-Ile (11.6), Dallo-N-Me-Ile (12.2), L-N-Me-Val (5.3) and D-N-Me-Val (8.5)in solvent A, L-Val (6.8), D-Val (18.3), L-Pro (4.9) and D-Pro(6.5) in solvent B. The retention times and ESIMS product ions(m/z [M+Na]+) of the L-FDAA derivatives of N-Me-Ile and NMe-Val from the hydrolysate were 6.6 min (420.1) and 5.3 min(406.1) in solvent A, respectively, proving the configurationsof N-Me-Ile and N-Me-Val were L. The retention times andESIMS product ions (m/z [M+Na]+) of the L-FDAA derivatives of Val and Pro from the hydrolysate were 6.8 min (392.1)and 4.9 min (390.1) in solvent B, respectively, proving theconfigurations of Val and Pro were L
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