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[ CAS No. 51-44-5 ] {[proInfo.proName]}

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Chemical Structure| 51-44-5
Chemical Structure| 51-44-5
Structure of 51-44-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 51-44-5 ]

CAS No. :51-44-5 MDL No. :MFCD00002492
Formula : C7H4Cl2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :VPHHJAOJUJHJKD-UHFFFAOYSA-N
M.W : 191.01 Pubchem ID :5817
Synonyms :

Calculated chemistry of [ 51-44-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.42
TPSA : 37.3 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.01 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.56
Log Po/w (XLOGP3) : 3.46
Log Po/w (WLOGP) : 2.69
Log Po/w (MLOGP) : 2.79
Log Po/w (SILICOS-IT) : 2.5
Consensus Log Po/w : 2.6

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -3.54
Solubility : 0.0549 mg/ml ; 0.000287 mol/l
Class : Soluble
Log S (Ali) : -3.92
Solubility : 0.0227 mg/ml ; 0.000119 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.01
Solubility : 0.188 mg/ml ; 0.000986 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.2

Safety of [ 51-44-5 ]

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

Application In Synthesis of [ 51-44-5 ]

* 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 [ 51-44-5 ]
  • Downstream synthetic route of [ 51-44-5 ]

[ 51-44-5 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 64-17-5 ]
  • [ 51-44-5 ]
  • [ 28394-58-3 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 1992, vol. 40, # 4, p. 1047 - 1049
[2] Angewandte Chemie - International Edition, 2007, vol. 46, # 10, p. 1627 - 1629
[3] Annales Academiae Scientiarum Fennicae, Series A2: Chemica, 1945, # 16,
[4] Arzneimittel-Forschung/Drug Research, 2008, vol. 58, # 10, p. 510 - 514
[5] Archiv der Pharmazie, 2017, vol. 350, # 9,
[6] RSC Advances, 2018, vol. 8, # 12, p. 6306 - 6314
  • 2
  • [ 64-17-5 ]
  • [ 6287-38-3 ]
  • [ 51-44-5 ]
  • [ 28394-58-3 ]
YieldReaction ConditionsOperation in experiment
61% With sodium cyanide In N,N-dimethyl-formamide at 50℃; for 1 h; Molecular sieve General procedure: Aldehyde 1 (1.0 mmol; 1.0 equiv.) and 4 ? molecular sieves (300 mg) were added to a mixture of DMF (3.0 mL) and an appropriate alcohol (or a thiol) (3.0 mL). To the above solution was added sodium cyanide (1.5 mmol; 1.5 equiv). The reaction mixture was stirred in an open flask at 50 C and monitored by TLC. After the complete consumption of 1, the mixture was poured into water (25 mL) and extracted with diethyl ether (5 × 10 mL). The organic layers were combined, dried over anhydrous magnesium sulfate, and concentrated. The crude mixture was further purified by column chromatography on silica gel using ethyl acetate/hexane as the eluent to furnish the desired ester compound 3. The aqueous layer was acidified with HCl, extracted with ether, and concentrated to yield the corresponding carboxylic acid 6, which was sufficiently pure needing no further purification.
Reference: [1] Bulletin of the Korean Chemical Society, 2015, vol. 36, # 8, p. 2055 - 2061
  • 3
  • [ 51-44-5 ]
  • [ 1569262-64-1 ]
  • [ 28394-58-3 ]
YieldReaction ConditionsOperation in experiment
71% for 120 h; Reflux General procedure: Sulfonimidate 1 (0.859 g, 3.00 mmol) and 2-bromobenzoic acid (0.601 g, 3.00 mmol) were refluxed in THF (25 mL) for 5 d. TLC analysis (hexane–EtOAc, 6:1) showed that most of 1 had been converted into the sulfonamide 2. The mixture was concentrated by rotary evaporation and pentane (5 mL) was added. The pentane solution was removed by pipet and treated with NaH to precipitate any unreacted acid and residual 2. This solution was pipet filtered, concentrated in vacuo and purified by Kugelrohr distillation; yield: 0.32 g (47percent). IR and 1H NMR spectra were identical to published spectra.
Reference: [1] Synthesis (Germany), 2013, vol. 45, # 24, p. 3361 - 3368
  • 4
  • [ 51-44-5 ]
  • [ 28394-58-3 ]
Reference: [1] Journal of Medicinal Chemistry, 1983, vol. 26, # 5, p. 765 - 768
  • 5
  • [ 51-44-5 ]
  • [ 1047953-91-2 ]
Reference: [1] Bioorganic and Medicinal Chemistry, 2018, vol. 26, # 12, p. 3321 - 3344
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