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[ CAS No. 5651-88-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 5651-88-7
Chemical Structure| 5651-88-7
Structure of 5651-88-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 5651-88-7 ]

CAS No. :5651-88-7 MDL No. :MFCD00026051
Formula : C9H8S Boiling Point : -
Linear Structure Formula :- InChI Key :HXKVNRKJSSHQQY-UHFFFAOYSA-N
M.W : 148.22 Pubchem ID :4131667
Synonyms :

Safety of [ 5651-88-7 ]

Signal Word:Danger Class:9
Precautionary Statements:P280-P302+P352+P312-P304+P340+P312-P273 UN#:3334
Hazard Statements:H312+H332-H413-H372 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 5651-88-7 ]

* 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 [ 5651-88-7 ]

[ 5651-88-7 ] Synthesis Path-Downstream   1~7

  • 2
  • [ 5651-88-7 ]
  • [ 89031-82-3 ]
  • [ 144512-05-0 ]
  • 3
  • [ 5651-88-7 ]
  • [ 38257-52-2 ]
  • [ 1209009-31-3 ]
  • 4
  • [ 5651-88-7 ]
  • [ 5219-61-4 ]
YieldReaction ConditionsOperation in experiment
72% With trimethylsilylazide; silver carbonate In dimethyl sulfoxide at 100℃; for 12h;
  • 5
  • [ CAS Unavailable ]
  • [ 5651-88-7 ]
  • [ 121-46-0 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
93% With dicobalt octacarbonyl; ethylene glycol In toluene at 80℃; stereoselective reaction; Catalytic Pauson-Khand Reaction; General Procedure B (GPB) General procedure: Catalytic Pauson-Khand Reaction; General Procedure A (GPA). In a flame-dried pressure tube containing a magnetic stirrer, the 1,6-enyne (100 mg, 1.0 equiv) or alkyne (100 mg, 1 equiv) was dissolved in anhyd toluene (0.3 M). Co2(CO)8 (5 mol% or 1 mol% as indicated) was added. In the case of intermolecular reactions, norbornadiene or norbornene (5.0 equiv) was also added. The pressure vessel was first purged with N2 and then with CO (3 ×). Finally, it was charged with CO (1-2 bar) and heated to 80 °C; the mixture was stirred overnight.The CO was removed using a vacuum line and the biphasic solution was concentrated under reduced pressure. The crude was purified by column chromatography (hexanes/EtOAc mixtures of increasing polarity). Catalytic Pauson-Khand Reaction; General Procedure B (GPB) As for GPA but MEG (15% v/v) was added to the mixture.
  • 6
  • [ 1809-10-5 ]
  • [ 5651-88-7 ]
  • (4-ethylhex-1-yn-3-yl)(phenyl)sulfane [ No CAS ]
YieldReaction ConditionsOperation in experiment
83% Stage #1: phenyl propargyl sulfide With n-butyllithium In tetrahydrofuran; hexane at -78 - 20℃; for 1h; Stage #2: 3-bromopentane In tetrahydrofuran; hexane at -78℃; for 2h;
  • 7
  • [ 14243-64-2 ]
  • [ 5651-88-7 ]
  • C27H22AuPS [ No CAS ]
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