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[ CAS No. 626-72-2 ] {[proInfo.proName]}

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Chemical Structure| 626-72-2
Chemical Structure| 626-72-2
Structure of 626-72-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 626-72-2 ]

CAS No. :626-72-2 MDL No. :MFCD00020391
Formula : C8H16N2O4S2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 268.35 Pubchem ID :-
Synonyms :
Chemical Name :(H-HoCys-OH)2

Calculated chemistry of [ 626-72-2 ]

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.75
Num. rotatable bonds : 9
Num. H-bond acceptors : 6.0
Num. H-bond donors : 4.0
Molar Refractivity : 64.71
TPSA : 177.24 Ų

Pharmacokinetics

GI absorption : Low
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) : -11.88 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.91
Log Po/w (XLOGP3) : -5.56
Log Po/w (WLOGP) : -0.03
Log Po/w (MLOGP) : -5.14
Log Po/w (SILICOS-IT) : -0.62
Consensus Log Po/w : -2.09

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 1.0
Egan : 1.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : 2.59
Solubility : 105000.0 mg/ml ; 392.0 mol/l
Class : Highly soluble
Log S (Ali) : 2.5
Solubility : 84200.0 mg/ml ; 314.0 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : 0.15
Solubility : 380.0 mg/ml ; 1.42 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.42

Safety of [ 626-72-2 ]

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

Application In Synthesis of [ 626-72-2 ]

* 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 [ 626-72-2 ]
  • Downstream synthetic route of [ 626-72-2 ]

[ 626-72-2 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 626-72-2 ]
  • [ 2314-97-8 ]
  • [ 764-52-3 ]
YieldReaction ConditionsOperation in experiment
93%
Stage #1: at -78 - 35℃; Inert atmosphere
Stage #2: at -78℃; for 0.333333 h;
FIRST EMBODIMENTIn a 500-ml three-necked flask equipped with a liquid-ammonia cooling device, a glass stirring bar, a thermometer, and a septum rubber cap was placed 10.0 g (37.3 mmol) of L-homocystine, followed by thorough purging of the flask with nitrogen. After cooling the flask to -78° C., ammonia which had been dried by passing through a KOH tube was liquefied in the liquid-ammonia cooling device cooled on a dry ice-acetone bath, and the liquid ammonia was added in a volume of about 100 ml to L-homocystine, followed by stirring. Next, 3.58 g (156 mmol) of metallic sodium was gradually added while avoiding rise of the temperature of the mixture above -35° C. The solution (mixture) became dark blue in this step. Next, 18.2 g (93.3 mmol) of trifluoromethyl iodide weighed using a balloon was added, the mixture was stirred on a bath at -78° C. for 20 minutes, from which ammonia was gradually evaporated, the residue was dissolved in ultrapure water, and the solution was placed on an ion exchange resin DOWEX-50X8 which had been treated with hydrochloric acid. After passing a sufficient amount of ultrapure water, elution with a 2percent aqueous ammonia solution was performed, and thereby yielded 14.1 g of target L-trifluoromethionine in a yield of 93percent.1H-NMR (D2O, 200 MHz) δ: 2.07-2.37 (m, 2H) , 3.01 (t, 2H, J=7.6 Hz), 4.03 (t, 1H, J=6.6 Hz)19F-NMR (D2O, 188 MHz) δ: -41.3 (s)
Reference: [1] Patent: US2011/15433, 2011, A1, . Location in patent: Page/Page column 4
[2] Journal of Fluorine Chemistry, 2011, vol. 132, # 3, p. 186 - 189
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