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[ CAS No. 100-76-5 ] {[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| 100-76-5
Chemical Structure| 100-76-5
Structure of 100-76-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 100-76-5 ]

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Product Details of [ 100-76-5 ]

CAS No. :100-76-5 MDL No. :MFCD00006690
Formula : C7H13N Boiling Point : No data available
Linear Structure Formula :HC(CH2CH2)3N InChI Key :SBYHFKPVCBCYGV-UHFFFAOYSA-N
M.W : 111.18 Pubchem ID :7527
Synonyms :

Safety of [ 100-76-5 ]

Signal Word:Danger Class:8,6.1
Precautionary Statements:P501-P270-P262-P264-P280-P302+P352-P332+P313-P362-P301+P310+P330-P302+P350+P310-P305+P351+P338+P310-P405 UN#:2923
Hazard Statements:H301-H310-H315-H318 Packing Group:Ⅱ
GHS Pictogram:

Application In Synthesis of [ 100-76-5 ]

* 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 [ 100-76-5 ]

[ 100-76-5 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 100-76-5 ]
  • [ 6608-47-5 ]
  • [ 39896-06-5 ]
  • 1-Aza-bicyclo[2.2.2]octane; compound with ethenesulfonic acid [ No CAS ]
  • [ 87323-99-7 ]
  • 2
  • [ 103260-44-2 ]
  • [ 100-76-5 ]
  • 3
  • [ 5344-27-4 ]
  • [ 100-76-5 ]
  • 4
  • [ 100-76-5 ]
  • [ 126-83-0 ]
  • 1-(3-sulfo-2-hydroxypropyl)quinuclidinium inner salt [ No CAS ]
YieldReaction ConditionsOperation in experiment
77% Preparation of 1-(3-sulfo-2-hydroxypropyl) quinuclidinium, inner salt (Compound JX); A solution of 3-chloro-2-hydroxy-1-propanesulfonic acid, sodium salt (2 g, 10 mmol) in water (12 mL total volume) was added over 1 hour to a mixture of quinuclidine (1.63 g, 4.7 mmol), water (10 mL) and 1,4-dioxane (10 mL) at 80 C. The mixture was stirred at this temperature for another 2 hours after the end of the addition. The reaction mixture was concentrated then the mixture was passed over a column of Dowex 50×8 (125 g). The fractions containing the pure product were concentrated to a white solid. The solid was dried for 18 hours at 60 C. in the vacuum oven. The desired material was obtained as a white solid (1.92 g, 7.7 mmol, 77%). The 1H and 13C NMR and MS were consistent with the structure.
  • 5
  • [ 100-76-5 ]
  • [ 13195-50-1 ]
  • [ 127-08-2 ]
  • [ 1173173-98-2 ]
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