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[ CAS No. 7064-31-5 ]

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Cat. No.: {[proInfo.prAm]}
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type HazMat fee
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Inaccessible (Haz class 6.1), Domestic USD 41.00
Inaccessible (Haz class 6.1), International USD 64.00
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Chemical Structure| 7064-31-5
Chemical Structure| 7064-31-5
Structure of 7064-31-5 * Storage: {[proInfo.prStorage]}
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Product Details of [ 7064-31-5 ]

CAS No. :7064-31-5 MDL No. :MFCD02183532
Formula : C9H6BrNO Boiling Point : -
Linear Structure Formula :- InChI Key :N/A
M.W :224.05 g/mol Pubchem ID :-
Synonyms :

Safety of [ 7064-31-5 ]

Signal Word:Danger Class:8,6.1
Precautionary Statements:P261-P280-P301+P310-P305+P351+P338 UN#:2923
Hazard Statements:H301-H315-H318-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 7064-31-5 ]

* 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.

  • Upstream synthesis route of [ 7064-31-5 ]
  • Downstream synthetic route of [ 7064-31-5 ]

[ 7064-31-5 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 1606168-00-6 ]
  • [ 7064-31-5 ]
  • [ 13484-04-3 ]
YieldReaction ConditionsOperation in experiment
41.2% With hydroxylamine hydrochloride In waterReflux General procedure: A solution of 0.62 g(0.009 mol) of hydroxylamine hydrochloride in a minimum amount of water was added to a saturated solution of 0.0015 mol of trans-1-(β-aroylvinyl)pyridiniumbromide in acetonitrile or methanol. Thereaction mixture was refluxed during 27–30 h, cooled,and poured into 200 mL of water. The reaction productswere extracted with chloroform and re-precipitatedwith diethyl ether. The resulting precipitate wasfiltered off, washed with ether, and dried in vacuum.
Reference: [1] Russian Journal of General Chemistry, 2015, vol. 85, # 5, p. 1078 - 1081[2] Russian Journal of General Chemistry, 2015, vol. 85, # 5, p. 1078 - 1081,4
  • 2
  • [ 73387-60-7 ]
  • [ 7064-31-5 ]
  • [ 13484-04-3 ]
Reference: [1] Journal of Heterocyclic Chemistry, 2008, vol. 45, # 3, p. 879 - 885
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