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[ CAS No. 492-30-8 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 492-30-8
Chemical Structure| 492-30-8
Chemical Structure| 492-30-8
Structure of 492-30-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 492-30-8 ]

CAS No. :492-30-8 MDL No. :MFCD07369541
Formula : C6H10O5 Boiling Point : -
Linear Structure Formula :- InChI Key :WJBVKNHJSHYNHO-ZMIZWQJLSA-N
M.W : 162.14 Pubchem ID :11805069
Synonyms :

Calculated chemistry of [ 492-30-8 ]

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.83
Num. rotatable bonds : 1
Num. H-bond acceptors : 5.0
Num. H-bond donors : 3.0
Molar Refractivity : 33.65
TPSA : 86.99 Ų

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) : -8.16 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.31
Log Po/w (XLOGP3) : -1.22
Log Po/w (WLOGP) : -1.98
Log Po/w (MLOGP) : -1.68
Log Po/w (SILICOS-IT) : -0.68
Consensus Log Po/w : -1.05

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -0.01
Solubility : 158.0 mg/ml ; 0.976 mol/l
Class : Very soluble
Log S (Ali) : -0.11
Solubility : 125.0 mg/ml ; 0.773 mol/l
Class : Very soluble
Log S (SILICOS-IT) : 0.8
Solubility : 1020.0 mg/ml ; 6.27 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.04

Safety of [ 492-30-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 492-30-8 ]

* 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.

  • Upstream synthesis route of [ 492-30-8 ]
  • Downstream synthetic route of [ 492-30-8 ]

[ 492-30-8 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 492-30-8 ]
  • [ 15397-15-6 ]
Reference: [1] ACS Medicinal Chemistry Letters, 2016, vol. 7, # 1, p. 17 - 22
[2] Patent: CN108440613, 2018, A,
  • 2
  • [ 492-30-8 ]
  • [ 98-88-4 ]
  • [ 874638-80-9 ]
YieldReaction ConditionsOperation in experiment
58%
Stage #1: With triethylamine In dichloromethaneCooling with ice
Stage #2: With pyridine; trifluoromethylsulfonic anhydride In dichloromethane at -40 - 20℃; for 1 h;
Stage #3: With triethylamine tris(hydrogen fluoride); triethylamine In acetonitrileCooling with ice
The 2-C-methyl-D- ribotide -1,4-lactone (0.32g, 2mmoL) suspended in 10 ml methylene chloride, under the condition of ice bath, dripping benzoyl chloride (0.46 ml, 4mmoL, 2eq). Is omitted, then slowly dripped into triethylamine (0.61 ml, 4 . 4mmoL, 2 . 2eq), at least 1 hour drop end, reaction sleepovers. Pyridine is added to the reaction system (0.18 ml, 2 . 2mmoL, 1 . 1eq), -40 ° C stirring, then slowly adding trifluoromethyl sulfonic anhydride (0.37 ml, 2 . 2mmoL, 1 . 1eq), after dripping, slowly to room temperature, is continuously stirred for 1 hour. Added to the reaction solution 1.5mLDMSO, stir at room temperature, TLC monitoring after the reaction is complete, concentrated reaction fluid to the surface of the small volume, added to the reaction system in acetonitrile (12 ml), triethylamine three hydrofluoric acid salt (0.49 ml, 3mmoL, 1.5eq) and triethylamine (1.40 ml, 10mmoL, 5eq), stirring under the conditions of ice, at this temperature into the sulfuryl fluoride gas. TLC monitoring after the reaction is complete, evaporate the solvent, by adding 20 ml of water, the room temperature is arranged to separate out reddish brown solid. Filtering, after drying, is obtained after beating with methanol 0.42g gray solid, yield 58percent.
Reference: [1] Patent: CN105693661, 2016, A, . Location in patent: Paragraph 0116; 0117; 0118; 0119
  • 3
  • [ 492-30-8 ]
  • [ 874638-80-9 ]
Reference: [1] Tetrahedron Letters, 2015, vol. 56, # 29, p. 4345 - 4348
[2] Tetrahedron Letters, 2015, vol. 56, # 29, p. 4345 - 4348
[3] Patent: CN105693661, 2016, A,
[4] Patent: CN105693661, 2016, A,
[5] Patent: CN105693661, 2016, A,
[6] Patent: CN105693661, 2016, A,
[7] Patent: CN105693661, 2016, A,
[8] Patent: CN105693661, 2016, A,
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