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[ CAS No. 66-84-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 66-84-2
Chemical Structure| 66-84-2
Structure of 66-84-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 66-84-2 ]

CAS No. :66-84-2 MDL No. :MFCD00135831
Formula : C6H14ClNO5 Boiling Point : -
Linear Structure Formula :- InChI Key :QKPLRMLTKYXDST-NSEZLWDYSA-N
M.W : 215.63 Pubchem ID :2723635
Synonyms :
D-(+)-Glucosamine hydrochloride;Chitosamine hydrochloride;NSC 758;NSC 234443;GlcN;D-(+)-Glucosamine;D-Glucosamine (hydrochloride)
Chemical Name :(2R,3R,4S,5R)-2-Amino-3,4,5,6-tetrahydroxyhexanal hydrochloride

Calculated chemistry of [ 66-84-2 ]

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.83
Num. rotatable bonds : 5
Num. H-bond acceptors : 6.0
Num. H-bond donors : 5.0
Molar Refractivity : 45.48
TPSA : 124.01 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) : -9.67 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : -2.89
Log Po/w (WLOGP) : -2.61
Log Po/w (MLOGP) : -2.56
Log Po/w (SILICOS-IT) : -1.84
Consensus Log Po/w : -1.98

Druglikeness

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

Water Solubility

Log S (ESOL) : 0.97
Solubility : 2030.0 mg/ml ; 9.41 mol/l
Class : Highly soluble
Log S (Ali) : 0.84
Solubility : 1500.0 mg/ml ; 6.97 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : 2.23
Solubility : 36800.0 mg/ml ; 171.0 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.13

Safety of [ 66-84-2 ]

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 [ 66-84-2 ]

* 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 [ 66-84-2 ]
  • Downstream synthetic route of [ 66-84-2 ]

[ 66-84-2 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 66-84-2 ]
  • [ 290-37-9 ]
  • [ 109-08-0 ]
  • [ 98-00-0 ]
  • [ 67-47-0 ]
  • [ 6705-31-3 ]
  • [ 55087-82-6 ]
Reference: [1] Journal of Agricultural and Food Chemistry, 1998, vol. 46, # 3, p. 1129 - 1131
  • 2
  • [ 1242172-32-2 ]
  • [ 58-86-6 ]
  • [ 50-99-7 ]
  • [ 59-23-4 ]
  • [ 66-84-2 ]
Reference: [1] Phytochemistry, 2010, vol. 71, # 11-12, p. 1375 - 1380
  • 3
  • [ 7512-17-6 ]
  • [ 66-84-2 ]
Reference: [1] Patent: US9267141, 2016, B2, . Location in patent: Page/Page column 14
  • 4
  • [ 9012-76-4 ]
  • [ 66-84-2 ]
Reference: [1] European Journal of Pharmacology, 2008, vol. 579, # 1-3, p. 74 - 85
  • 5
  • [ 3006-60-8 ]
  • [ 66-84-2 ]
  • [ 4704-14-7 ]
Reference: [1] Journal of the Chemical Society, 1957, p. 81,85
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