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[ CAS No. 50-69-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 50-69-1
Chemical Structure| 50-69-1
Structure of 50-69-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 50-69-1 ]

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Product Details of [ 50-69-1 ]

CAS No. :50-69-1 MDL No. :
Formula : C5H10O5 Boiling Point : -
Linear Structure Formula :HOCH2CH(OH)CH(OH)CH(OH)CHO InChI Key :PYMYPHUHKUWMLA-LMVFSUKVSA-N
M.W : 150.13 Pubchem ID :5311110
Synonyms :
Chemical Name :(2R,3R,4R)-2,3,4,5-Tetrahydroxypentanal

Calculated chemistry of [ 50-69-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.8
Num. rotatable bonds : 4
Num. H-bond acceptors : 5.0
Num. H-bond donors : 4.0
Molar Refractivity : 31.0
TPSA : 97.99 ?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 : Yes
Log Kp (skin permeation) : -8.86 cm/s

Lipophilicity

Log Po/w (iLOGP) : -3.66
Log Po/w (XLOGP3) : -2.32
Log Po/w (WLOGP) : -2.74
Log Po/w (MLOGP) : -2.48
Log Po/w (SILICOS-IT) : -1.29
Consensus Log Po/w : -2.5

Druglikeness

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

Water Solubility

Log S (ESOL) : 0.95
Solubility : 1350.0 mg/ml ; 9.01 mol/l
Class : Highly soluble
Log S (Ali) : 0.8
Solubility : 944.0 mg/ml ; 6.29 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : 1.94
Solubility : 13000.0 mg/ml ; 86.9 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.81

Safety of [ 50-69-1 ]

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

Application In Synthesis of [ 50-69-1 ]

* 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 [ 50-69-1 ]

[ 50-69-1 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 1005-39-6 ]
  • [ 50-69-1 ]
  • D-ribose-(6-amino-2-methylsulfanyl-pyrimidin-4-ylimine) [ No CAS ]
  • 2
  • [ 50-69-1 ]
  • [ 24259-59-4 ]
  • [ 50-69-1 ]
  • 3
  • [ 50-69-1 ]
  • [ 7149-75-9 ]
  • D-ribose-(4-chloro-3-methyl-phenylimine) [ No CAS ]
  • 4
  • [ 557-01-7 ]
  • [ 50-69-1 ]
  • [ 65025-04-9 ]
  • [ 3690-10-6 ]
  • [ 65025-05-0 ]
  • 6
  • [ 50-69-1 ]
  • [ 24259-59-4 ]
  • DL-ribose [ No CAS ]
  • 7
  • [ 1500092-25-0 ]
  • [ 50-69-1 ]
  • [ 24259-59-4 ]
  • [ 50-99-7 ]
  • [ 921-60-8 ]
YieldReaction ConditionsOperation in experiment
With trifluoroacetic acid; In water; at 120℃; for 4h; Compound 1 (about 4 mg) was added into a solution of water (1 mL) and 2N aqueous CF3COOH(2 mL), heated to 120°C under reflux conditions for 4 h. The mixture was diluted with water (2 mL) and then extracted with EtOAc (3 £2 mL). The combined organic phase was washed with brine and evaporated to dryness to afford the aglycones. The aqueous phase was concentrated. Then dry pyridine (1 mL) and L-cysteine methyl ester hydrochloride (2 mg) were added into the residue. Each mixture was reacted at 60°C for 1 h, and 0.5mL of (trimethylsilyl) imidazole dissolved in H2O was added, followed by heating to dryness at 60°C for 2 h. Each dried reactant was extracted with n-hexane (3 £ 1 mL) and H2O (1 mL, each). The n-hexane fraction was subjected to GC (column: Rtx-1, 0.25mm i.d. 0.25 mm, length 30 m). The conditions of GC were flame ionization detector; column temperature 100?180°C (10°C min?1)and 180?230°C (3°C min21); injector temperature 250°C; detector temperature 300°C and the carrier gas (N2, 0.8mLmin21). Under these conditions, these sugars of each reactants were identified by comparison with authentic samples: tR (min) 7.56 (D-ribose), 7.85 (L-ribose), 10.49 (D-glucose) and 11.10 (L-glucose).
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