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[ CAS No. 13515-93-0 ] {[proInfo.proName]}

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Chemical Structure| 13515-93-0
Chemical Structure| 13515-93-0
Structure of 13515-93-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 13515-93-0 ]

CAS No. :13515-93-0 MDL No. :MFCD00038876
Formula : C4H10ClNO2 Boiling Point : -
Linear Structure Formula :CH3NHCH2CO2CH3·HCl InChI Key :HQZMRJBVCVYVQA-UHFFFAOYSA-N
M.W : 139.58 Pubchem ID :83544
Synonyms :
Chemical Name :Methyl N-methylglycinate hydrochloride

Calculated chemistry of [ 13515-93-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.75
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 32.39
TPSA : 38.33 ?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) : -6.78 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.52
Log Po/w (WLOGP) : 0.18
Log Po/w (MLOGP) : 0.01
Log Po/w (SILICOS-IT) : -0.35
Consensus Log Po/w : 0.07

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.84
Solubility : 20.4 mg/ml ; 0.146 mol/l
Class : Very soluble
Log S (Ali) : -0.9
Solubility : 17.7 mg/ml ; 0.127 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.73
Solubility : 26.2 mg/ml ; 0.188 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.03

Safety of [ 13515-93-0 ]

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 [ 13515-93-0 ]

* 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 [ 13515-93-0 ]
  • Downstream synthetic route of [ 13515-93-0 ]

[ 13515-93-0 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 24424-99-5 ]
  • [ 13515-93-0 ]
  • [ 42492-57-9 ]
YieldReaction ConditionsOperation in experiment
90% With triethylamine In dichloromethane at 0 - 20℃; for 48 h; Inert atmosphere To a suspension of sarcosine (35.64 g, 0.40 mol) in 350 mL MeOH was added thionyl chloride (29.02 mL, 0.40 mol) dropwise at 0 °C. After complete addition the cooling bath was removed and the reaction mixture was stirred for 30 min at r.t. and refluxed for further 6 h. The resulting solution was concentrated in vacuum and the residue was dried in high vacuum over night at r.t. to afford sarcosine methyl ester.HCl as a white powder which was used in the next step without further purification; yield: 56.14 g (quant.); mp. 102 °C. 1H-NMR (300 MHz, CDCl3): δ = 9.76 (s, 2 H, NH2), 3.88 (t, J = 5.6 Hz, 2 H, H-2), 3.82 (s, 3 H, H-4)), 2.83 (t, J = 5.2 Hz, 3 H, H-3). 13C-NMR(75 MHz, CDCl3): δ = 166.7 (C-1), 53.3 (C-2), 48.9 (C-3), 33.4 (C-4).1 To a suspension of sarcosine methylester.HCl (59.80 g, 0.43 mol) and (Boc)2O (138.01 mL, 0.65 mol) in 1.0 L CH2Cl2 TEA (119.09 mL, 0.86 mol) was added dropwise at 0 °C. After complete addition the cooling bath was removed and the reaction mixture was stirred for two days at r.t. Aq. HCl (1 M) was added until the aqueous layer showed pH = 6. The resulting two layers were separated and the organic layer was washed with dist. H2O, dried (Na2SO4), concentrated in vacuum and volatile impurities were removed in high vacuum over night at r.t. to afford a clear oil; yield: 78.65 g (90 percent)
Reference: [1] Synthesis (Germany), 2017, vol. 49, # 4, p. 770 - 774
[2] Patent: EP1032561, 2004, B1, . Location in patent: Page 21
  • 2
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  • [ 42492-57-9 ]
Reference: [1] Gazzetta Chimica Italiana, 1977, vol. 107, p. 381 - 385
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