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[ CAS No. 2140-72-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 2140-72-9
Chemical Structure| 2140-72-9
Structure of 2140-72-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 2140-72-9 ]

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Product Details of [ 2140-72-9 ]

CAS No. :2140-72-9 MDL No. :MFCD11519076
Formula : C10H15N3O5 Boiling Point : -
Linear Structure Formula :- InChI Key :RFCQJGFZUQFYRF-ZOQUXTDFSA-N
M.W : 257.24 Pubchem ID :150971
Synonyms :
2'-O-Methylcytidine
Chemical Name :2'-O-Methylcytidine

Calculated chemistry of [ 2140-72-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.6
Num. rotatable bonds : 3
Num. H-bond acceptors : 6.0
Num. H-bond donors : 3.0
Molar Refractivity : 60.58
TPSA : 119.83 ?2

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) : -9.0 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.12
Log Po/w (XLOGP3) : -1.59
Log Po/w (WLOGP) : -2.23
Log Po/w (MLOGP) : -1.58
Log Po/w (SILICOS-IT) : -1.77
Consensus Log Po/w : -1.21

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.48
Solubility : 84.8 mg/ml ; 0.33 mol/l
Class : Very soluble
Log S (Ali) : -0.42
Solubility : 98.3 mg/ml ; 0.382 mol/l
Class : Very soluble
Log S (SILICOS-IT) : 0.31
Solubility : 525.0 mg/ml ; 2.04 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 4.01

Safety of [ 2140-72-9 ]

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 [ 2140-72-9 ]

* 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 [ 2140-72-9 ]

[ 2140-72-9 ] Synthesis Path-Upstream   1~18

  • 1
  • [ 73793-16-5 ]
  • [ 2140-72-9 ]
Reference: [1] Journal of Organic Chemistry, 1982, vol. 47, # 2, p. 202 - 206
  • 2
  • [ 1085342-86-4 ]
  • [ 2140-72-9 ]
Reference: [1] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 19, p. 8795 - 8800
  • 3
  • [ 97626-19-2 ]
  • [ 2140-72-9 ]
Reference: [1] Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 1986, vol. 40, # 10, p. 826 - 830
  • 4
  • [ 17287-03-5 ]
  • [ 65-46-3 ]
  • [ 20594-00-7 ]
  • [ 2140-72-9 ]
  • [ 2140-64-9 ]
Reference: [1] Journal of Organic Chemistry, 1980, vol. 45, # 19, p. 3865 - 3868
[2] Journal of Organic Chemistry, 1980, vol. 45, # 19, p. 3865 - 3868
[3] Journal of Organic Chemistry, 1980, vol. 45, # 19, p. 3865 - 3868
[4] Journal of the Chemical Society, Perkin Transactions 1, 1980, p. 2787 - 2792
[5] Journal of the Chemical Society, Perkin Transactions 1, 1980, p. 2787 - 2792
  • 5
  • [ 65-46-3 ]
  • [ 74-88-4 ]
  • [ 2140-72-9 ]
Reference: [1] Patent: US5646265, 1997, A,
  • 6
  • [ 2414-98-4 ]
  • [ 2140-72-9 ]
Reference: [1] Organic Process Research and Development, 2000, vol. 4, # 3, p. 170 - 171
  • 7
  • [ 684-93-5 ]
  • [ 65-46-3 ]
  • [ 2140-72-9 ]
  • [ 2140-64-9 ]
Reference: [1] Angewandte Chemie - International Edition, 2018, vol. 57, # 20, p. 5943 - 5946[2] Angew. Chem., 2018, vol. 130, # 20, p. 6050 - 6054,5
  • 8
  • [ 68045-07-8 ]
  • [ 2140-72-9 ]
Reference: [1] Journal of Organic Chemistry, 1982, vol. 47, # 2, p. 202 - 206
  • 9
  • [ 22224-41-5 ]
  • [ 2140-72-9 ]
Reference: [1] Journal of Organic Chemistry, 1982, vol. 47, # 2, p. 202 - 206
  • 10
  • [ 17287-03-5 ]
  • [ 65-46-3 ]
  • [ 20594-00-7 ]
  • [ 2140-72-9 ]
Reference: [1] Bulletin of the Chemical Society of Japan, 1986, vol. 59, p. 2947 - 2949
[2] Bulletin of the Chemical Society of Japan, 1986, vol. 59, p. 2947 - 2949
  • 11
  • [ 1899-02-1 ]
  • [ 65-46-3 ]
  • [ 2140-69-4 ]
  • [ 20594-00-7 ]
  • [ 2140-72-9 ]
Reference: [1] Synthetic Communications, 1980, vol. 10, # 1, p. 25 - 36
[2] Synthetic Communications, 1980, vol. 10, # 1, p. 25 - 36
  • 12
  • [ 108782-90-7 ]
  • [ 2140-72-9 ]
Reference: [1] Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 1986, vol. 40, # 10, p. 826 - 830
  • 13
  • [ 110567-19-6 ]
  • [ 2140-72-9 ]
Reference: [1] Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 1986, vol. 40, # 10, p. 826 - 830
  • 14
  • [ 415903-48-9 ]
  • [ 2140-72-9 ]
Reference: [1] Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 1986, vol. 40, # 10, p. 826 - 830
  • 15
  • [ 69304-38-7 ]
  • [ 2140-72-9 ]
Reference: [1] Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 1986, vol. 40, # 10, p. 826 - 830
  • 16
  • [ 65-46-3 ]
  • [ 74-88-4 ]
  • [ 20594-00-7 ]
  • [ 2140-72-9 ]
Reference: [1] Journal of Organic Chemistry, 1991, vol. 56, # 20, p. 5846 - 5859
[2] Journal of Organic Chemistry, 1991, vol. 56, # 20, p. 5846 - 5859
  • 17
  • [ 121-43-7 ]
  • [ 10212-28-9 ]
  • [ 2140-72-9 ]
Reference: [1] Tetrahedron, 2000, vol. 56, # 8, p. 1047 - 1056
  • 18
  • [ 186581-53-3 ]
  • [ 65-46-3 ]
  • [ 20594-00-7 ]
  • [ 2140-72-9 ]
Reference: [1] Helvetica Chimica Acta, 1996, vol. 79, # 8, p. 2114 - 2136
[2] Carbohydrate Research, 1981, vol. 91, p. 31 - 38
[3] Carbohydrate Research, 1981, vol. 91, p. 31 - 38
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