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[ CAS No. 20312-37-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 20312-37-2
Chemical Structure| 20312-37-2
Structure of 20312-37-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 20312-37-2 ]

CAS No. :20312-37-2 MDL No. :MFCD00211263
Formula : C6H12O3 Boiling Point : -
Linear Structure Formula :- InChI Key :LVRFTAZAXQPQHI-RXMQYKEDSA-N
M.W : 132.16 Pubchem ID :439960
Synonyms :
D-α-Hydroxyisocaproic acid
Chemical Name :(R)-2-Hydroxy-4-methylpentanoic acid

Calculated chemistry of [ 20312-37-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.83
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 33.89
TPSA : 57.53 ?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) : -6.5 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.19
Log Po/w (XLOGP3) : 0.86
Log Po/w (WLOGP) : 0.48
Log Po/w (MLOGP) : 0.39
Log Po/w (SILICOS-IT) : 0.09
Consensus Log Po/w : 0.6

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.0
Solubility : 13.1 mg/ml ; 0.0993 mol/l
Class : Very soluble
Log S (Ali) : -1.65
Solubility : 2.95 mg/ml ; 0.0223 mol/l
Class : Very soluble
Log S (SILICOS-IT) : 0.08
Solubility : 159.0 mg/ml ; 1.2 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.63

Safety of [ 20312-37-2 ]

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

Application In Synthesis of [ 20312-37-2 ]

* 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.

  • Downstream synthetic route of [ 20312-37-2 ]

[ 20312-37-2 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1342309-23-2 ]
  • [ 17407-56-6 ]
  • [ 17407-55-5 ]
  • [ 312-84-5 ]
  • [ 56-45-1 ]
  • [ 20312-37-2 ]
  • [ 13748-90-8 ]
  • [ 3060-46-6 ]
  • [ 63-91-2 ]
  • [ 31321-74-1 ]
  • [ 673-06-3 ]
  • 2
  • [ 1342309-24-3 ]
  • [ 17407-56-6 ]
  • [ 17407-55-5 ]
  • [ 312-84-5 ]
  • [ 56-45-1 ]
  • [ 20312-37-2 ]
  • [ 13748-90-8 ]
  • [ 3060-46-6 ]
  • [ 63-91-2 ]
  • [ 31321-74-1 ]
  • [ 673-06-3 ]
  • 3
  • [ 20312-37-2 ]
  • [ 41036-32-2 ]
  • C16H23NO4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
98% With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 0 - 20℃; To a soln of D-Alanine benzyl ester p-toluene sulfonate (58.50 g, 167 mmol) in acetonitrile anhyd (100 mL) was dropwised DIPEA (44.97 g, 348 mmol) in acetonitrile anhyd (50 mL) at 0 C. The mixture was added D-O-leucine (20.00 g, 151 mmol) in acetonitrile anhyd (50 mL), EDCI hydrochloride (34.81 g, 182 mmol) and HOBt (20.45 g, 151 mmol) and stirred at r.t. over night. The reaction mixture was then evaporated concentrated under reduced pressure. The residue was washed sequentially 10% citric acid (3 × 300 mL), sat. NaHCO3 soln (3 × 300 mL) and brine (3 × 300 mL). The organic layer was dried over Na2SO4, filtered and concentrated under redued pressure. The crude residue was purified by silica gel chromatography (hexane-EtOAc, 9:1) and recrystallized from EtOAc-hexane as a white solid; yield: 43.58 g (98%); mp 60.5-61.7 C, [a]D25 +47.29 (c 1.00, CHCl3). IR (KBr film):3385, 3323, 2956, 2870, 1743, 1643, 1529, 1464, 1398, 1294, 1163, 1083, 742, 697. 1H NMR (CDCl3, 400 MHz): delta = 0.94 (d, J=2.4 Hz, 3H), 0.96 (d, J=2.4 Hz, 3H), 1.43 (d, J=7.2 Hz, 3H), 1.43-1.66 (m, 2H), 1.84-1.86 (m, 1H), 2.82 (s, 1H), 4.14-4.17 (m, 1H), 4.63-4.66 (m, 1H), 5.14 (dd, J=12.4, 5.2 Hz, 2H), 6.99 (d, J=11.5 Hz, 1H), 7.33-7.39 (m, 5H). ESI-MS: m/z [M+H]+ calcd for C16H24NO4: 294.1705; found: 294.1737.
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