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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
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Inaccessible (Haz class 6.1), International USD 150+
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Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 3057-04-3 Chemical Structure| 3057-04-3

Structure of 3057-04-3

Chemical Structure| 3057-04-3

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Product Details of [ 3057-04-3 ]

CAS No. :3057-04-3
Formula : C25H42O4
M.W : 406.60
SMILES Code : O[C@@H]1CC[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@H]([C@H](C)CCC(OC)=O)CC[C@@]4([H])[C@]3([H])[C@H](O)CC2C1
MDL No. :MFCD00232923

Safety of [ 3057-04-3 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301+H311+H331
Precautionary Statements:P501-P261-P270-P271-P264-P280-P361+P364-P301+P310+P330-P302+P352+P312-P304+P340+P311-P403+P233-P405
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 3057-04-3 ]

* 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 [ 3057-04-3 ]

[ 3057-04-3 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 3057-04-3 ]
  • [ 10538-59-7 ]
YieldReaction ConditionsOperation in experiment
96.9% With copper nanoparticles on activated carbon; dihydrogen peroxide; In benzene; for 4h;Reflux; The 40g goosey deoxycholic acid methyl ester is dissolved in 400 ml phenyltheophylline in, input 3.1g copper activated charcoal in, stir, continue adding 20 ml after the hydrogen peroxide is, reflux reaction 4 hours; cooling down to room temperature, contained in filtered to remove catalyst copper activated charcoal, 90 C the lower vacuum concentration benzene solution, to obtain 3 alpha-hydroxy-7-carbonyl -5 beta- cholane acid methyl ester 39.9g, content is 96.9%;
74.1% With silica gel; pyridinium chlorochromate; In dichloromethane; at 20℃;Cooling with ice; Step B To three 500mL flask was added compound 2 (4.06g, 10mmol) and DCM 125mL, stirred clear solution, silica gel was added to the reaction solution 20g (200-300 mesh), DCM was added dropwise under ice-water bath containing PCC (2.4 g PCC was dissolved in 125mL DCM), the reaction warmed to room temperature after dropwise, TLC detection reaction to the raw material after the reaction, was filtered, residue washed with DCM and filtrate and washings were combined, successively washed with water (100 mL x 2), saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, spin dried to give 3.0g of compound 3. Yield: 74.1%.
40.2 g With oxygen; In butan-1-ol; for 5h;Irradiation; 40.6 g methyl chenodeoxycholate was dissolved in 200 mL n-butanol,And the solution was placed in a 0.5 mol / L solution. Then 16.7 g were addedTetraiodofluoresceinAs sensitizers,Stirring dissolved completely;The mixed solution was placed in a hard glass tube,Pass into the pure oxygen saturation, stopper closed;400w high pressure sodium lamp continuous irradiation for 5 hours,Stop lighting,HPLC analysis showed that the consumption of methyl chenodeoxycholate was complete, indicating complete reaction.100 mL of a saturated sodium carbonate solution was added to the reaction mixture which had been completely reacted at room temperature,Washing to remove sensitizers,At 70 recovered butanol layer was concentrated under vacuum,getHydroxy-7-oxo-5beta-Choline acidMethyl ester40.2 g, content of 97.1%
  • 2
  • [ 10538-59-7 ]
  • [ 927-77-5 ]
  • [ 3057-04-3 ]
  • methyl 7-propyl-chenodeoxycholate [ No CAS ]
  • 3
  • [ 10538-59-7 ]
  • [ 10538-55-3 ]
  • [ 3057-04-3 ]
  • 4
  • [ 10538-59-7 ]
  • [ 3057-04-3 ]
  • 6
  • [ 3057-04-3 ]
  • [ 14773-00-3 ]
  • [ 10538-59-7 ]
  • [ 7753-72-2 ]
  • 7
  • [ 3057-04-3 ]
  • [ 10538-59-7 ]
  • [ 7753-72-2 ]
YieldReaction ConditionsOperation in experiment
62%; 31% With silica gel; pyridinium chlorochromate; In chloroform; at 20℃; for 5h;Inert atmosphere; To a solution of methyl-3alpha,7alpha-dihydroxy-5beta-cholanoate (Compound 2; 500 mg, 1.23 mmol) in CHCl3 (30 mL, anhydrous) was added silica-gel (2 g) and to this suspension was then added pyridinium chlorochromate (300 mg, 1.38 mmol). The reaction was stirred at room temperature for 5 hours under nitrogen atmosphere. Et2O was added (100 mL) and the suspension was filtered over a silica-gel column eluting with Et2O/DCM (7/3) to afford the desired product as a colorless solid (309 mg, 62%). MS (ESI+): m/z 427.1[M+Na]+. By-product methyl-3,7-di-oxo-5beta-cholanoate was obtained as a colorless solid (154 mg, 31%). MS (ESI+): m/z 425.2[M+Na]+.
 

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