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[ CAS No. 623-51-8 ] {[proInfo.proName]}

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Chemical Structure| 623-51-8
Chemical Structure| 623-51-8
Structure of 623-51-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 623-51-8 ]

CAS No. :623-51-8 MDL No. :MFCD00004874
Formula : C4H8O2S Boiling Point : -
Linear Structure Formula :HSCH2C(O)OCH2CH3 InChI Key :PVBRSNZAOAJRKO-UHFFFAOYSA-N
M.W : 120.17 Pubchem ID :12185
Synonyms :

Calculated chemistry of [ 623-51-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.75
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 30.56
TPSA : 65.1 ?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) : -6.47 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.65
Log Po/w (XLOGP3) : 0.8
Log Po/w (WLOGP) : 0.48
Log Po/w (MLOGP) : 0.49
Log Po/w (SILICOS-IT) : 0.58
Consensus Log Po/w : 0.8

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.89
Solubility : 15.4 mg/ml ; 0.129 mol/l
Class : Very soluble
Log S (Ali) : -1.75
Solubility : 2.14 mg/ml ; 0.0178 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.83
Solubility : 17.9 mg/ml ; 0.149 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.4

Safety of [ 623-51-8 ]

Signal Word:Danger Class:3,6.1
Precautionary Statements:P301+P310-P305+P351+P338 UN#:1992
Hazard Statements:H225-H301-H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 623-51-8 ]

* 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 [ 623-51-8 ]
  • Downstream synthetic route of [ 623-51-8 ]

[ 623-51-8 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 623-51-8 ]
  • [ 10191-60-3 ]
  • [ 39736-29-3 ]
YieldReaction ConditionsOperation in experiment
99% With diisopropylamine In N,N-dimethyl-formamide at 100℃; for 5 h; The synthesis of ethyl 4-amino-2-(methylthio)thiazole-5-carboxylate
Ethyl 2-mercaptoacetate (50 g, 0.416 mol) was dissolved in 500 ml of dimethylformamide and added with dimethyl N-thienodithioimino carbonate (67 g, 0.416 mol) and diisopropylamine (112 ml, 0.624 mol).
After heating at 100° C. for 5 hours, the mixture was extracted with 500 ml of saturated ammonium chloride and 500 ml of ethylacetate, dried with sodium sulfate, filtered and concentrated under vacuum.
After washing the solid with n-hexane, the title compound (90 g, 99percent) was obtained.
1H-NMR (400 MHz, CDCl3); δ 5.84 (brs, 2H), 4.26 (q, J=7.2 Hz, 2H), 2.63 (s, 3H), 1.32 (t, J=7.2 Hz, 3H); LC-MS 219 (MH+)
89% With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 100℃; Ethyl 2-mercaptoacetate (5 g, 42 mmol, 1.0 eq) was dissolved in DMF (50 mL) and added with N-thienodi-thioimino carbonate (6.1 g, 42 mmol, 1.0 eq) and DIPEA (16.3 g, 126 mmol, 3.0 eq). After heating at 100 °C for 5 h, the mixture was diluted with saturated aqueous ammonium chloride (100 mL) and extracted with EtOAc (100 mLx2). The combined organic layer was washed with brine, dried, concentrated. The solid was washed with n-hexane and dried under vacuum to give the title compound (8 g, yield: 89percent) as a yellow solid. ESI-MS (M+H)+: 219.0.
Reference: [1] Patent: US2013/72482, 2013, A1, . Location in patent: Paragraph 0315-0317
[2] Patent: WO2015/89327, 2015, A1, . Location in patent: Paragraph 0468
[3] Tetrahedron Letters, 1966, # 17, p. 1885 - 1889
[4] Patent: WO2015/193506, 2015, A1, . Location in patent: Page/Page column 57-58
  • 2
  • [ 623-51-8 ]
  • [ 39736-29-3 ]
Reference: [1] Patent: US5326776, 1994, A,
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