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[ CAS No. 145-42-6 ] {[proInfo.proName]}

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Chemical Structure| 145-42-6
Chemical Structure| 145-42-6
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Product Details of [ 145-42-6 ]

CAS No. :145-42-6 MDL No. :MFCD00150819
Formula : C26H44NNaO7S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 537.68 Pubchem ID :-
Synonyms :
Chemical Name :Sodium 2-((R)-4-((3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-trihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanamido)ethane-1-sulfonate (1:1)

Safety of [ 145-42-6 ]

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 [ 145-42-6 ]

* 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 [ 145-42-6 ]

[ 145-42-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 15366-32-2 ]
  • [ 145-42-6 ]
  • amino((2-ethoxy-2-oxoethyl)(methyl)amino)methaniminium 2-((R)-4-((3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-trihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanamido)ethane-1-sulfonate [ No CAS ]
YieldReaction ConditionsOperation in experiment
95% In ethanol; at 50℃; for 4h; To the solution of CEE hydrochloride 22(1.0 mmol, 0.195 g) in EtCH (15 mL) equimolar quantity of sodium taurocholate hydrate 24(1 .0 mmol, 0.538 g) was added and the mixture was then stirred for 4h at the 50 C. Sodium chloride, formed during the reaction, was separated by filtration through the 22 micron membrane filter and the filtrate was taken to dryness. Diethyl ether was added to the product and after evaporation, product 26 was isolated as white solid in quantitative yield.White solid (95%, 0.641 g, 0.95 mmol). M.p. 179.4-195.4 C; 1H NMR (500 MHz,CD3OD, 5)4.27-4.23 (m, 1H), 4.19 (5, 1H), 3.95 (5, 1H), 3.79 (5, 1H), 3.58 (t, J= 7.0 Hz,2H), 3.49 (q, J= 7.0 Hz, 1H), 3.40-3.35 (m, 2H), 3.19 (5, 2H), 3.07 (5, 1H), 2.96 (t, J= 3.0Hz, 2H), 2.31-2.23 (m, 3H), 2.14-2.07 (m, 1H), 2.02-1.92 (m, 2H), 1.90-1.83 (m, 2H), 1.82-1.71 (m, 3H), 1.67-1.61.4 (m, 1H), 1.61-1.51 (m, 5H), 1.43-1.26 (m, 6H), 1.17 (t, J= 7.1, 2H),1.12-1.09 (m, 1H), 1.03 (d, J= 6.1 Hz, 2H), 0.98-0.95 (m, 2H), 0.91 (5, 3H), 0.71 (brs, 3H).l3 NMR (125 MHz, CD3OD) O 177.0, 169.8, 160.0, 74.5, 73.3, 69.5, 63.4, 58.8, 53.1, 52.0,48.5, 48.0, 43.6, 43.5, 41.5, 40.9, 38.4, 37.4, 37.1, 36.4, 34.7, 33.6, 31.7, 30.1, 29.1, 28.3,24.7, 23.7, 18.9, 18.3, 14.9, 13.5. HRMS(ESI) calcd for C6H14N302 [M+H] 160.1081, found160.1080; HRMS (ESI) calcd for C26H44N075 [M-H]- 514.2844, found 514.2830.
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