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[ CAS No. 2002-24-6 ] {[proInfo.proName]}

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Chemical Structure| 2002-24-6
Chemical Structure| 2002-24-6
Structure of 2002-24-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2002-24-6 ]

CAS No. :2002-24-6 MDL No. :MFCD00012892
Formula : C2H8ClNO Boiling Point : -
Linear Structure Formula :H2NC2H4OH·HCl InChI Key :PMUNIMVZCACZBB-UHFFFAOYSA-N
M.W : 97.54 Pubchem ID :74819
Synonyms :
Chemical Name :2-Aminoethanol hydrochloride

Calculated chemistry of [ 2002-24-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 5
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 22.56
TPSA : 46.25 ?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) : -7.26 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : -0.51
Log Po/w (WLOGP) : -0.26
Log Po/w (MLOGP) : -0.63
Log Po/w (SILICOS-IT) : -0.88
Consensus Log Po/w : -0.46

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.06
Solubility : 85.5 mg/ml ; 0.876 mol/l
Class : Very soluble
Log S (Ali) : 0.01
Solubility : 99.1 mg/ml ; 1.02 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : 0.42
Solubility : 254.0 mg/ml ; 2.61 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 2002-24-6 ]

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 [ 2002-24-6 ]

* 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 [ 2002-24-6 ]

[ 2002-24-6 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 534-22-5 ]
  • [ 2002-24-6 ]
  • [ 22099-62-3 ]
  • 2
  • [ 4497-29-4 ]
  • [ 2002-24-6 ]
  • [ 7450-26-2 ]
  • 9
  • [ 2002-24-6 ]
  • [ 870-24-6 ]
YieldReaction ConditionsOperation in experiment
98% With thionyl chloride; In N-methyl-acetamide; water; benzene; EXAMPLE 7 A mixture of 975 g. of <strong>[2002-24-6]monoethanolamine hydrochloride</strong>, 3.7 g. of dimethylformamide and 3500 g. of benzene was heated to 75 to 80C., and 1404 g. of thionylchloride were added dropwise thereto over 7 hours at the same temperature. After the addition was completed, the reaction solution was kept at the same temperature for further 1 hour and cooled to 30C., and then 2900 g. of water was added thereto. Then the solution was allowed to stand to separate into the benzene and aqueous layers. 4150 g. of the aqueous layer thus obtained contained 2-chloroethylamine hydrochloride which was produced in 98 % of yield, and 2.7 % by weight of free sulfur dioxide based on the aqueous layer.
95% With thionyl chloride; In toluene; at 75℃; for 3h; Reagents and reaction conditions: SOCl2, Toluene, 75 Necked flask was added 15.0g of ethanolamine hydrochloride M-07 and toluene 15mL, stirring in an oil bath heated to 75 , the pressure-equalizing dropping funnel was slowly added dropwise 20.0g of thionyl chloride, the reaction ends after 3h. Cooling to room temperature, suction filtered, the filter cake was washed with a small amount of toluene and the toluene filtrate recovery next reuse. The filter cake was dried in vacuo to give a white solid 2-chloro-ethylamine hydrochloride 16.9g, that is, M-08, 95% yield.
  • 10
  • [ 2002-24-6 ]
  • [ 151-50-8 ]
  • [ 108-94-1 ]
  • [ 54961-36-3 ]
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