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[ CAS No. 27243-15-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 27243-15-8
Chemical Structure| 27243-15-8
Structure of 27243-15-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 27243-15-8 ]

CAS No. :27243-15-8 MDL No. :MFCD11044492
Formula : C6H6ClNO4 Boiling Point : -
Linear Structure Formula :- InChI Key :OWZGNRBFMASABS-UHFFFAOYSA-N
M.W : 191.57 Pubchem ID :12535337
Synonyms :

Calculated chemistry of [ 27243-15-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.5
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 42.13
TPSA : 63.68 ?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) : -7.58 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.16
Log Po/w (XLOGP3) : -0.15
Log Po/w (WLOGP) : -0.55
Log Po/w (MLOGP) : 0.5
Log Po/w (SILICOS-IT) : 0.46
Consensus Log Po/w : 0.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.74
Solubility : 35.2 mg/ml ; 0.184 mol/l
Class : Very soluble
Log S (Ali) : -0.73
Solubility : 35.4 mg/ml ; 0.185 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.82
Solubility : 29.3 mg/ml ; 0.153 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.2

Safety of [ 27243-15-8 ]

Signal Word:Danger Class:8
Precautionary Statements:P260-P264-P270-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P405-P501 UN#:3261
Hazard Statements:H302-H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 27243-15-8 ]

* 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.

  • Downstream synthetic route of [ 27243-15-8 ]

[ 27243-15-8 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 6066-82-6 ]
  • [ 79-04-9 ]
  • [ 27243-15-8 ]
YieldReaction ConditionsOperation in experiment
53% With triethylamine; In chloroform; at 0℃; for 0.416667h; To a solution of N-hydroxysuccinimide (640.3 mg, 5.56 mmol) in chloroform (8.5 mL) was added triethylamine (861.6 mu, 6.18 mmol) 0 C. Then, a-chloroacetyl chloride was added dropwise over a 5 minute period and stirred for an additional 20 minutes at 0C. The reaction mixture was washed with ice-cold water (15 mL) and brine (15 mL), concentrated to a volume of 1.7 mL in vacuo, then dried with sodium sulfate and filtered. To the resulting solution were added ethyl acetate (170 mu) and hexanes (1.2 mL), and the mixture was cooled down to 0 C stirred for 2 h, and a white solid was precipitated. It was filtered and washed first with ice-cold 10 mL portion of hexanes/ethyl acetate (4: 1), then with 10 mL hexanes/ethyl acetate (9: 1), and finally with hexanes (10 mL, twice). The resulting white solid was dried under house vacuum to yield 2,5-dioxopyrrolidin-l-yl 2-chloroacetate (563.9 mg, 53%). NMR 400 MHz (CDC13) delta 4.37 (s, 2H), 2.87 (s, 4H).
  • 2
  • [ 27243-15-8 ]
  • [ 142182-02-3 ]
  • [ 142182-09-0 ]
  • 3
  • [ 27243-15-8 ]
  • [ 79677-63-7 ]
  • 1-(N-benzyloxycarbonyl-3-iodo-L-tyrosyl)-2-chloroacetylhydrazine [ No CAS ]
  • 4
  • [ 27243-15-8 ]
  • 7-aminomethyl-1-azathioxanthone [ No CAS ]
  • 7-(N-methyl-2-chloro-acetamide)-1-azathioxanthone [ No CAS ]
  • 5
  • [ 27243-15-8 ]
  • [ 1004751-65-8 ]
  • [ 1004751-66-9 ]
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