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[ CAS No. 79-07-2 ] {[proInfo.proName]}

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Chemical Structure| 79-07-2
Chemical Structure| 79-07-2
Structure of 79-07-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 79-07-2 ]

CAS No. :79-07-2 MDL No. :MFCD00008027
Formula : C2H4ClNO Boiling Point : No data available
Linear Structure Formula :- InChI Key :VXIVSQZSERGHQP-UHFFFAOYSA-N
M.W : 93.51 Pubchem ID :6580
Synonyms :
Chemical Name :2-Chloroacetamide

Calculated chemistry of [ 79-07-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 5
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.5
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 19.43
TPSA : 43.09 ?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) : -7.25 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.39
Log Po/w (XLOGP3) : -0.53
Log Po/w (WLOGP) : -0.29
Log Po/w (MLOGP) : -0.37
Log Po/w (SILICOS-IT) : 0.07
Consensus Log Po/w : -0.15

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.02
Solubility : 89.3 mg/ml ; 0.955 mol/l
Class : Very soluble
Log S (Ali) : 0.09
Solubility : 116.0 mg/ml ; 1.24 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.4
Solubility : 37.2 mg/ml ; 0.398 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.04

Safety of [ 79-07-2 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P501-P261-P273-P272-P270-P202-P201-P264-P280-P302+P352-P308+P313-P362+P364-P333+P313-P301+P310+P330-P405 UN#:2811
Hazard Statements:H301-H317-H361-H402 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 79-07-2 ]

* 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 [ 79-07-2 ]
  • Downstream synthetic route of [ 79-07-2 ]

[ 79-07-2 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 120-83-2 ]
  • [ 79-07-2 ]
  • [ 27320-99-6 ]
Reference: [1] Journal of the Korean Chemical Society, 2012, vol. 56, # 4, p. 468 - 472,5
[2] Journal of the Korean Chemical Society, 2012, vol. 56, # 4, p. 468 - 472
  • 2
  • [ 121-33-5 ]
  • [ 79-07-2 ]
  • [ 186685-89-2 ]
YieldReaction ConditionsOperation in experiment
86% With potassium carbonate In N,N-dimethyl-formamide; acetonitrileReflux General procedure: A mixture of the corresponding halide (0.010 mol), hydroxybenzaldehyde (0.011 mol), and potassium carbonate (2.00 g, 0.0145 mol) in a mixture of acetonitrile-DMF (20 mL, 8 : 2, v/v) was refluxed for 5-7 h with stirring (TLC monitoring). After evaporation of the solvents, the residue was treated with water, a precipitate formed was filtered off, washed with 30percent aqueous methanol, and dried in air. Yields and physicochemical characteristics of aldehydes 9-12 are given in Table 4.
Reference: [1] Russian Chemical Bulletin, 2015, vol. 64, # 2, p. 395 - 404[2] Izv. Akad. Nauk, Ser. Khim., 2015, # 2, p. 395 - 404,10
[3] Russian Journal of General Chemistry, 2005, vol. 75, # 7, p. 1113 - 1124
[4] European Journal of Medicinal Chemistry, 2014, vol. 81, p. 1 - 14
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