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[ CAS No. 57641-66-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 57641-66-4
Chemical Structure| 57641-66-4
Structure of 57641-66-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 57641-66-4 ]

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Product Details of [ 57641-66-4 ]

CAS No. :57641-66-4 MDL No. :MFCD20621572
Formula : C4H9BrO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :JTOJLOUPDKBCCH-UHFFFAOYSA-N
M.W : 169.02 Pubchem ID :11819432
Synonyms :
Chemical Name :2-(2-Bromoethoxy)ethanol

Calculated chemistry of [ 57641-66-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 4
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 31.46
TPSA : 29.46 ?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) : -7.22 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.76
Log Po/w (XLOGP3) : 0.15
Log Po/w (WLOGP) : 0.39
Log Po/w (MLOGP) : 0.42
Log Po/w (SILICOS-IT) : 0.83
Consensus Log Po/w : 0.71

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.72
Solubility : 32.3 mg/ml ; 0.191 mol/l
Class : Very soluble
Log S (Ali) : -0.33
Solubility : 79.9 mg/ml ; 0.473 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.51
Solubility : 5.22 mg/ml ; 0.0309 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.32

Safety of [ 57641-66-4 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 57641-66-4 ]

* 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 [ 57641-66-4 ]
  • Downstream synthetic route of [ 57641-66-4 ]

[ 57641-66-4 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 111-46-6 ]
  • [ 57641-66-4 ]
YieldReaction ConditionsOperation in experiment
12%
Stage #1: With triphenylphosphine In dichloromethane at 20℃; for 0.5 h;
Stage #2: With carbon tetrabromide In dichloromethane at 20℃;
A solution of 2,2'-oxydiethanol (25 g, 236 mmol) in DCM (250 mL) was treated with triphenylphosphine (30.9 g, 1 18 mmol) and the solution was stirred at room temperature for 30 min. Carbon tetrabromide (39.1 g, 1 18 mmol) was added to the solution dropwise over 60 min. then mixture was stirred at 20 °C overnight. The mixture was evaporated and purified by chromatography (silica gel, 0.2-0.33percent EtOAc in pet. ether) to afford the desired product (5.0 g; 12percent) as a colorless oil. LCMS m/z 192.9 and 190.8 (M+Na)+, 170.9 and 168.8 (M+H)+
Reference: [1] Angewandte Chemie - International Edition, 2014, vol. 53, # 48, p. 13196 - 13200[2] Angew. Chem., 2014, vol. 126, # 48, p. 13412 - 13416,5
[3] Journal of Organic Chemistry, 1993, vol. 58, # 27, p. 7694 - 7699
[4] Journal of Medicinal Chemistry, 2012, vol. 55, # 15, p. 6898 - 6915
[5] Angewandte Chemie - International Edition, 2005, vol. 44, # 34, p. 5480 - 5483
[6] Organic and Biomolecular Chemistry, 2008, vol. 6, # 14, p. 2554 - 2559
[7] Patent: WO2019/53617, 2019, A1, . Location in patent: Page/Page column 177
[8] Patent: WO2009/94242, 2009, A1, . Location in patent: Page/Page column 33
  • 2
  • [ 75-21-8 ]
  • [ 540-51-2 ]
  • [ 57641-66-4 ]
Reference: [1] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 25, p. 865
  • 3
  • [ 75-21-8 ]
  • [ 540-51-2 ]
  • [ 57641-67-5 ]
  • [ 57641-66-4 ]
Reference: [1] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 25, p. 865
  • 4
  • [ 107-21-1 ]
  • [ 106-93-4 ]
  • [ 57641-66-4 ]
Reference: [1] Annales de Chimie (Cachan, France), 1863, vol. <3>67, p. 272
  • 5
  • [ 107-21-1 ]
  • [ 106-93-4 ]
  • [ 123-91-1 ]
  • [ 57641-67-5 ]
  • [ 57641-66-4 ]
  • [ 540-51-2 ]
Reference: [1] Annales de Chimie (Cachan, France), 1863, vol. <3>67, p. 272
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