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[ CAS No. 36155-85-8 ] {[proInfo.proName]}

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Chemical Structure| 36155-85-8
Chemical Structure| 36155-85-8
Structure of 36155-85-8 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 36155-85-8 ]

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Product Details of [ 36155-85-8 ]

CAS No. :36155-85-8 MDL No. :MFCD17016115
Formula : C5H3ClOS Boiling Point : -
Linear Structure Formula :- InChI Key :BGOGYRKWKJGOHZ-UHFFFAOYSA-N
M.W : 146.60 Pubchem ID :12284899
Synonyms :

Calculated chemistry of [ 36155-85-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 34.72
TPSA : 45.31 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.75 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.59
Log Po/w (XLOGP3) : 2.03
Log Po/w (WLOGP) : 2.21
Log Po/w (MLOGP) : 1.01
Log Po/w (SILICOS-IT) : 3.34
Consensus Log Po/w : 2.04

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.42
Solubility : 0.552 mg/ml ; 0.00376 mol/l
Class : Soluble
Log S (Ali) : -2.61
Solubility : 0.36 mg/ml ; 0.00246 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.21
Solubility : 0.906 mg/ml ; 0.00618 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.14

Safety of [ 36155-85-8 ]

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 [ 36155-85-8 ]

* 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 [ 36155-85-8 ]

[ 36155-85-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 57002-01-4 ]
  • [ 36155-85-8 ]
  • [ 1448434-22-7 ]
YieldReaction ConditionsOperation in experiment
53% With tetrabutylammomium bromide; palladium diacetate; potassium carbonate; triphenylphosphine; In isopropyl alcohol; at 70℃; for 20h;Inert atmosphere; £6L ?(RI ?5) tE6 2 (9p-oswu ?ZRN oot) WIN RT (%o6? FE) PJaA MOJJa( ajUd U SU (01) auajj AU QuatpU1SauUxaJ-oyQ3 %oc-%oE) £qdU1OwwO1qo JSU £q uot-Uogun alnSSald paonpai iapun pawauaouoo UU tOStUNSflO1p(quU laAo paup SUM IaJ(UJ otUU1Q Qw os) arnaop(a UU (jw os) OtR uaaaq pauotpnUd puU alnSSaldpaonpai iapun papmuaouoo tN iapun Srnoq o IOJ D00L U 1fl3S SUM ainjxnu uOl3oUal aj Qowm 9L0 ? oo) Eq SUM (jounu OE ?R01d1 U? w) EQy ?Qoanu810 ? too) t(vo)Pd ?Qoww 91 ? oE) (6) ap(qapJUutJ-OotdOwOlq-9 ?Qoanu 091 ? tLi (5) ptcrn otuOlOqQi(utAp(-xajopi(o-j-() jo ainpctw PW1flJUS UO1U UU oi :1 dais(Rd ?m) 0IU9EI ?(Rd ?w) SdI-tSI ?(RI ?w) 9I9 ?(RI ?ZR 91=1 ?P) td9 ?(RI ?ZR 091 ?89=f ?PP) 98L ?(RI ?ZR T8=1 ?P) 69L ?(RI ?ZR T8=1 ?P) ILL ?(RI ?ZR 9L=f ?1) Step 1: Coupling of <strong>[57002-01-4](E)-(2-cyclohexylvinyl)boronic acid</strong> with 5-chlorothiophene-3-carbaldehyde in the presence of tetrabutylamonium bromide (1.2 g, 3.72 mmol) following the method used in Example 3 gave after flash chromatography purification (10%-50% EtOAc-hexanes gradient) (E)-5-(2-cyclohexylvinyl)thiophene-3-carbaldehyde as a yellow oil. Yield (0.4 g, 53%); 1H NMR (400 MHz, DMSO-d6) delta 9.77 (s, 1H), 8.38 (s, 1H), 7.29 (s, 1H), 6.55 (d, J=8.0 Hz, 1H), 6.13 (dd, J=16.4, 6.8 Hz, 1H), 2.08-2.02 (m, 1H), 1.80-1.58 (m, 5H), 1.38-1.08 (m, 5H).
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