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[ CAS No. 6027-21-0 ] {[proInfo.proName]}

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Chemical Structure| 6027-21-0
Chemical Structure| 6027-21-0
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Product Details of [ 6027-21-0 ]

CAS No. :6027-21-0 MDL No. :MFCD00077786
Formula : C4H9NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :UKAUYVFTDYCKQA-GSVOUGTGSA-N
M.W : 119.12 Pubchem ID :2724170
Synonyms :
Chemical Name :H-D-Homoser-OH

Calculated chemistry of [ 6027-21-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.75
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 3.0
Molar Refractivity : 26.98
TPSA : 83.55 ?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) : -10.14 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.33
Log Po/w (XLOGP3) : -4.38
Log Po/w (WLOGP) : -1.22
Log Po/w (MLOGP) : -3.46
Log Po/w (SILICOS-IT) : -1.19
Consensus Log Po/w : -1.98

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 3.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : 2.38
Solubility : 28500.0 mg/ml ; 239.0 mol/l
Class : Highly soluble
Log S (Ali) : 3.24
Solubility : 207000.0 mg/ml ; 1740.0 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : 0.87
Solubility : 887.0 mg/ml ; 7.45 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.68

Safety of [ 6027-21-0 ]

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

Application In Synthesis of [ 6027-21-0 ]

* 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 [ 6027-21-0 ]
  • Downstream synthetic route of [ 6027-21-0 ]

[ 6027-21-0 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 348-67-4 ]
  • [ 6027-21-0 ]
YieldReaction ConditionsOperation in experiment
50%
Stage #1: With methyl iodide In methanol; water at 20℃; for 48 h;
Stage #2: for 15 h; Reflux
According to a literature procedure,19D-methionine (1) (25.0 g,167.5 mmol, 1 equiv) was suspended in H2O/MeOH (466 mL/66 mL), and methyl iodide (25.2 mL, 405.4 mmol, 2.4 equiv) wasadded. The resulting suspension was stirred vigorously at roomtemperature for 48 h. Then the volume of the reaction mixturewas reduced to one-third by evaporation under vacuo and alongwith this, excess of methyl iodide was also removed. Water(155 mL) was added to the remaining reaction mixture followedby NaHCO3 (14.07 g, 167.5 mmol, 1 equiv). The resulting solutionwas refluxed for 15 h and cooled to room temperature. Solventwas removed under vacuo to yield thick syrup. This was dissolvedin water (45 mL) with heating. Addition of acetone (90 mL) followedby ethanol (1000 mL) resulted in the precipitation of a whitesolid, which was filtered and dried under vacuum to give 2 aswhite solid. Yield: 9.9 g (83 mmol, 50percent). Mp 202 C. 1H NMR(300 MHz, D2O): d = 1.92–1.78 (m, 1H, 3-CH), 2.09–2.92 (m, 1H,3-CH), 3.65–3.58 (m, 2H, 4-CH2), 3.68 (dd, 3JH,H = 4.8, 3JH,H = 7.5 Hz,1H, 2-CH). 13C NMR (75 MHz, D2O): d = 32.1 (s, 3-C), 53.3 (s, 2-C),58.5 (s, 4-C), 174.5 (s, 1-C). HRMS (ESI+, MeOH): m/z = 142.0468[M+Na]+ calcd for C4H9NO3Na+ 142.0475.
Reference: [1] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 19, p. 5168 - 5181
[2] Tetrahedron, 1988, vol. 44, # 2, p. 637 - 642
  • 2
  • [ 3493-10-5 ]
  • [ 6027-21-0 ]
Reference: [1] Journal of the American Chemical Society, 2009, vol. 131, p. 7917 - 7927
  • 3
  • [ 206194-18-5 ]
  • [ 6027-21-0 ]
Reference: [1] Tetrahedron, 2002, vol. 58, # 47, p. 9621 - 9628
  • 4
  • [ 104347-13-9 ]
  • [ 6027-21-0 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 1996, vol. 44, # 12, p. 2322 - 2325
  • 5
  • [ 50-00-0 ]
  • [ 338-69-2 ]
  • [ 6027-21-0 ]
Reference: [1] ACS Catalysis, 2017, vol. 7, # 3, p. 1707 - 1711
  • 6
  • [ 328-50-7 ]
  • [ 1927-25-9 ]
  • [ 6027-21-0 ]
  • [ 6893-26-1 ]
  • [ 56-86-0 ]
Reference: [1] Advanced Synthesis and Catalysis, 2014, vol. 356, # 17, p. 3505 - 3509
  • 7
  • [ 51744-82-2 ]
  • [ 6027-21-0 ]
Reference: [1] Archives of Biochemistry, 1953, vol. 42, p. 212,214
  • 8
  • [ 41088-89-5 ]
  • [ 6027-21-0 ]
  • [ 110045-70-0 ]
Reference: [1] Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences, 2004, vol. 59, # 4, p. 451 - 467
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