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[ CAS No. 5768-55-8 ]

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Chemical Structure| 5768-55-8
Chemical Structure| 5768-55-8
Structure of 5768-55-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 5768-55-8 ]

CAS No. :5768-55-8 MDL No. :MFCD11870772
Formula : C8H12N2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W :136.19 g/mol Pubchem ID :-
Synonyms :

Safety of [ 5768-55-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
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Application In Synthesis of [ 5768-55-8 ]

* 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 [ 5768-55-8 ]

[ 5768-55-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5768-55-8 ]
  • [ 701298-97-7 ]
YieldReaction ConditionsOperation in experiment
81% With N-Bromosuccinimide In tetrachloromethane for 1h; 93.a N-bromosuccinimide (1.3 g) was added to a solution of 6,7,8,9-tetrahydro-5H-imidazo[1,2-a]azepine (Hua, D. H. et al., J. Org. Chem., 59, 5084 (1994)) (1.0 g) in carbon tetrachloride (20 mL) and stirred for 1 hour. After an aqueous saturated sodium bicarbonate solution was added, the reaction solution was extracted with chloroform. The extract was dried over anhydrous sodium sulfate and then concentrated. The resulting residue was purified with a silica gel column to obtain the title compound (1.29 g, 81%) as a pale yellow solid. NMR (300 MHz, CDCl3) δ: 1.66-1.90 (6H, m), 2.89-2.93 (2H,m), 3.98 (2H, t, J = 4.8), 6.80 (1H, s).
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