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[ CAS No. 28868-76-0 ] {[proInfo.proName]}

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Chemical Structure| 28868-76-0
Chemical Structure| 28868-76-0
Structure of 28868-76-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 28868-76-0 ]

CAS No. :28868-76-0 MDL No. :MFCD00042837
Formula : C5H7ClO4 Boiling Point : -
Linear Structure Formula :- InChI Key :LNBQBURECUEBKZ-UHFFFAOYSA-N
M.W : 166.56 Pubchem ID :120070
Synonyms :

Calculated chemistry of [ 28868-76-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.6
Num. rotatable bonds : 4
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 33.52
TPSA : 52.6 ?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) : -6.71 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.76
Log Po/w (XLOGP3) : 0.86
Log Po/w (WLOGP) : -0.06
Log Po/w (MLOGP) : 0.25
Log Po/w (SILICOS-IT) : 0.47
Consensus Log Po/w : 0.66

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.15
Solubility : 11.8 mg/ml ; 0.0707 mol/l
Class : Very soluble
Log S (Ali) : -1.55
Solubility : 4.71 mg/ml ; 0.0283 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.69
Solubility : 34.0 mg/ml ; 0.204 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.84

Safety of [ 28868-76-0 ]

Signal Word:Danger Class:8
Precautionary Statements:P261-P264-P271-P273-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P391-P403+P233-P405-P501 UN#:3265
Hazard Statements:H314-H335-H400 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 28868-76-0 ]

* 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.

  • Downstream synthetic route of [ 28868-76-0 ]

[ 28868-76-0 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 3034-47-7 ]
  • [ 28868-76-0 ]
  • 2-(2-Chloro-5-nitro-thiazol-4-yl)-malonic acid dimethyl ester [ No CAS ]
  • 2
  • [ 28868-76-0 ]
  • [ 3034-48-8 ]
  • 2-(2-Bromo-5-nitro-thiazol-4-yl)-malonic acid dimethyl ester [ No CAS ]
  • 3
  • [ 28868-76-0 ]
  • [ 51419-59-1 ]
YieldReaction ConditionsOperation in experiment
a) p-Tolyl-methanesulfonyl chloride was prepared by oxidising commercially available p-tolyl-methanethiol with N-chlorosuccinimide in analogy to the procedure disclosed in [9].
  • 4
  • [ 28868-76-0 ]
  • [ 57297-29-7 ]
  • 5-chloro-2-cyclopropyl-4-hydroxy-1H-pyrimidin-6-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
30% With sodium methylate; In methanol; at 80℃; for 2h; (0583) (0584) [00234] To a solution of cyclopropanecarboxamidine (hydrochloride salt) in methanol (5 mL) was added sodium methoxide (16.4 mL of 0.5 M, 8.200 mmol) followed by dimethyl 2-chloropropanedioate (approximately 1.366 g, 1.047 mL, 8.200 mmol). The reaction mixture was heated to 80 °C for approximately 2 hours. The reaction was cooled to room temperature and partially concentrated until a solid appeared. The reaction mixture was acidified with ammonium chloride and dichloromethane was added. The resulting mixture was filtered and the precipitate was washed with diethyl ether to provide 5-chloro-2-cyclopropyl-4-hydroxy-lH- pyrimidin-6-one (458 mg, 30percent) as an off white solid. XH NMR (400 MHz, DMSO- d6) delta 12.46 (s, 1H), 7.31 - 6.93 (m, 1H), 1.89 (m, 1H), 1.06 (m, 4H) ppm. ESI-MS m/z calc. 186.0196, found 187.06 (M+l)+ ; Retention time: 0.44 minutes.
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