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[ CAS No. 102-54-5 ] {[proInfo.proName]}

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Chemical Structure| 102-54-5
Chemical Structure| 102-54-5
Structure of 102-54-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 102-54-5 ]

CAS No. :102-54-5 MDL No. :MFCD00001427
Formula : Fe(C5H5)2 Boiling Point : -
Linear Structure Formula :- InChI Key :KTWOOEGAPBSYNW-UHFFFAOYSA-N
M.W : 186.03 Pubchem ID :7611
Synonyms :

Calculated chemistry of [ 102-54-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.2
Num. rotatable bonds : 0
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 38.12
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -8.56 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : -1.67
Log Po/w (WLOGP) : 1.4
Log Po/w (MLOGP) : 3.08
Log Po/w (SILICOS-IT) : 1.98
Consensus Log Po/w : 0.96

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 3.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : 0.12
Solubility : 233.0 mg/ml ; 1.32 mol/l
Class : Highly soluble
Log S (Ali) : 2.18
Solubility : 26700.0 mg/ml ; 152.0 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -2.24
Solubility : 1.02 mg/ml ; 0.00578 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.59

Safety of [ 102-54-5 ]

Signal Word:Danger Class:4.1
Precautionary Statements:P210-P260-P280-P301+P312+P330-P370+P378 UN#:1325
Hazard Statements:H228-H302+H332-H361-H373-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 102-54-5 ]

* 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 [ 102-54-5 ]

[ 102-54-5 ] Synthesis Path-Downstream   1~23

  • 2
  • [ 102-54-5 ]
  • [ 38414-01-6 ]
  • [ 80937-33-3 ]
  • [ 12125-80-3 ]
  • [ 14172-90-8 ]
  • 3
  • [ 102-54-5 ]
  • [ 14172-90-8 ]
  • [ 80937-33-3 ]
  • [ 12125-80-3 ]
  • [ 38414-01-6 ]
  • 4
  • [ 1273-73-0 ]
  • [ 102-54-5 ]
Reference: [1]Doklady Akademii nauk SSSR,1964,vol. 154/159,p. 1213 - 1216
    Doklady Akademii Nauk SSSR,1964,vol. 159,p. 591 - 594
[2]Bulletin of the Chemical Society of Japan,1971,vol. 44,p. 808 - 812
[3]Bulletin of the Chemical Society of Japan,1971,vol. 44,p. 808 - 812
[4]Doklady Akademii nauk SSSR,1964,vol. 154/159,p. 30 - 32
    Doklady Akademii Nauk SSSR,1964,vol. 154,p. 158 - 159
[5]Nippon Kagaku Zasshi,
    Nippon Kagaku Zasshi,1970,vol. 91,p. A 33 - A 33
[6]Journal of Organic Chemistry,1961,vol. 26,p. 1034 - 1037
[7]Gmelin Handbuch der Anorganischen Chemie,Gmelin Handbook: Fe: Org.Verb.A1, 2.1.3, page 24 - 28
[8]Gmelin Handbuch der Anorganischen Chemie,Gmelin Handbook: Fe: Org.Verb.A1, 2.1.3, page 24 - 28
[9]Doklady Akademii nauk SSSR,1964,vol. 154/159,p. 30 - 32
    Doklady Akademii Nauk SSSR,1964,vol. 154,p. 158 - 159
[10]Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya,1963,p. 597 - 603
    Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya,1963,p. 667 - 674
[11]Journal of Organic Chemistry,1961,vol. 26,p. 1802 - 1805
[12]Bulletin of the Chemical Society of Japan,1969,vol. 42,p. 1976 - 1981
[13]Bulletin of the Chemical Society of Japan,1969,vol. 42,p. 1976 - 1981
[14]Doklady Akademii nauk SSSR,1965,vol. 160/165,p. 1121 - 1123
    Doklady Akademii Nauk SSSR,1965,vol. 165,p. 575 - 577
[15]Gmelin Handbuch der Anorganischen Chemie,Gmelin Handbook: Fe: Org.Verb.A1, 5.1.2.1.5, page 372 - 380
[16]Doklady Akademii nauk SSSR,1964,vol. 154/159,p. 765 - 768
    Doklady Akademii Nauk SSSR,1964,vol. 157,p. 922 - 925
  • 5
  • [ 29786-93-4 ]
  • [ 1273-73-0 ]
  • [ 15599-91-4 ]
  • [ 102-54-5 ]
  • N3P3F5(η-C5H4)Fe(η-C5H5) [ No CAS ]
  • [ 84462-68-0 ]
  • 6
  • [ 29786-93-4 ]
  • [ 1273-73-0 ]
  • [ 14700-00-6 ]
  • [ 102-54-5 ]
  • N4P4F7(η-C5H4)Fe(η-C5H5) [ No CAS ]
  • [ 89179-01-1 ]
  • 7
  • [ 126-33-0 ]
  • [ 102-54-5 ]
  • 1-cyanoferrocene [ No CAS ]
  • 9
  • [ 1273-73-0 ]
  • C5H5FeC5H4NHC6H5 [ No CAS ]
  • [ 102-54-5 ]
  • ((C5H5)Fe(C5H4))2N(C6H5) [ No CAS ]
  • 10
  • [ 1293-65-8 ]
  • 1-ethyl-1'-bromoferrocene [ No CAS ]
  • [ 102-54-5 ]
  • 1-ethylferrocene [ No CAS ]
  • 1',1'''-diethylbiferrocene [ No CAS ]
  • [ 211239-38-2 ]
  • 11
  • [ 102-54-5 ]
  • [ 191980-54-8 ]
  • [ 936484-37-6 ]
  • 12
  • [ 102-54-5 ]
  • [ 18995-35-2 ]
  • [ 143-66-8 ]
  • (η6-4-chlorophenyl-tert-butyl ether)(η5-cyclopentadienyl)iron(II) tetraphenylborate [ No CAS ]
  • 13
  • [ 102-54-5 ]
  • [ 23351-91-9 ]
  • [ 1075734-59-6 ]
  • 15
  • [ 1293-65-8 ]
  • [ 7732-18-5 ]
  • [ 102-54-5 ]
  • [ 1273-73-0 ]
  • 16
  • [ 79-27-6 ]
  • [ 1293-65-8 ]
  • [ 102-54-5 ]
  • [ 238413-86-0 ]
  • 18
  • [ 102-54-5 ]
  • [ 72040-64-3 ]
  • 6-biotinamidohexanoylferrocene [ No CAS ]
  • 19
  • [ 102-54-5 ]
  • [ 89889-51-0 ]
  • 6-(6-biotinamidohexanamido)hexanoylferrocene [ No CAS ]
  • 20
  • [ 102-54-5 ]
  • [ 124-73-2 ]
  • [ 1293-65-8 ]
  • 21
  • [ 102-54-5 ]
  • [ 174508-31-7 ]
  • 2,5-Diferrocenyl-3,4-ethylenedioxythiophene [ No CAS ]
  • 22
  • [ 1532-71-4 ]
  • [ 102-54-5 ]
  • [ 879559-36-1 ]
  • 23
  • [ 102-54-5 ]
  • [ 171243-30-4 ]
  • 3-fluoro-5-(trifluoromethyl)benzoyl ferrocene [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% With aluminum (III) chloride; In dichloromethane; at 20℃; for 2.83333h;Cooling; General procedure: A thoroughly dried two-necked round bottom flask was equipped with a mechanical stirrer. The system was maintained under pressure via dry nitrogen. The flask was charged with fer- rocene, fluorine/tri-fluoromethyl benzoyl chloride in 1:1 equiva- lent ratio and 11 ml of dichloride methane. The resulting mixture was stirred and the flask was immersed in an ice bath. When the solution has been thoroughly cooled, anhydrous AlCl 3 was added slowly for a period of about 20 min. A deep blue color indicates that the reaction has occurred and after its formation, stirring is continued for another 30 min with ice cooling. This is continued further for another 2 h at room temperature to ensure comple- tion of reaction. The reaction mixture was cooled again in ice, fol- lowed by continuous addition of 20 ml of water. The resulting two- phase mixture was stirred vigorously for 30 min. After transfer- ring the mixture to a separatory funnel, the layers are separated and the aqueous layer is extracted with two 20 ml portions of dichloromethane. The combined DCM solution was washed with 20 ml water, twice with 10 ml portions of 10% aq. NaOH and dried over anhydrous Na 2 SO 4 . The resulting solution was evapo- rated to dryness at reduced pressure, yielding the final product. The amount/volume of starting materials taken and the amount of the final synthesized compounds obtained is given in Table S1. The yields and obtained melting points (from DSC) are as follows: : 76%; 105 0 C; : 84%; 110 0 C; : 84%; 100 0 C; : 73%; 100 0 C; : 65%; 145 0 C ; : 70%; 65 0 C;
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