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[ CAS No. 6240-01-3 ] {[proInfo.proName]}

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Chemical Structure| 6240-01-3
Chemical Structure| 6240-01-3
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Product Details of [ 6240-01-3 ]

CAS No. :6240-01-3 MDL No. :MFCD01825827
Formula : C11H18ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :CMUAQGBJDDHTPE-UHFFFAOYSA-N
M.W : 231.72 Pubchem ID :365220
Synonyms :

Safety of [ 6240-01-3 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 6240-01-3 ]

* 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 [ 6240-01-3 ]

[ 6240-01-3 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 6240-00-2 ]
  • [ 34859-74-0 ]
  • [ 6240-01-3 ]
  • 2
  • [ 20866-48-2 ]
  • [ 6240-01-3 ]
  • [ 895167-08-5 ]
  • 3
  • [ 67-56-1 ]
  • [ 6240-01-3 ]
  • [ 80103-18-0 ]
  • 4
  • [ 6240-01-3 ]
  • [ 948045-15-6 ]
  • 5
  • [ 6240-01-3 ]
  • N,N'-bis(3-aminoadamantane-1-carboxylic acid)oxalamide [ No CAS ]
  • 7
  • [ 6240-01-3 ]
  • 3-[(S)-2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-adamantane-1-carboxylic acid [ No CAS ]
  • 8
  • [ 6240-01-3 ]
  • (S)-2-[(S)-2-({3-[(S)-2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-adamantane-1-carbonyl}-amino)-3-phenyl-propionylamino]-4-methylsulfanyl-butyric acid [ No CAS ]
  • 9
  • [ 6240-01-3 ]
  • [ 895167-19-8 ]
  • 10
  • [ 28920-43-6 ]
  • [ 6240-01-3 ]
  • [ 875211-10-2 ]
  • 11
  • [ 6240-01-3 ]
  • [ 501-53-1 ]
  • [ 10002-15-0 ]
  • 12
  • [ 6240-00-2 ]
  • [ 6240-01-3 ]
YieldReaction ConditionsOperation in experiment
78% With hydrogenchloride; water; at 95℃; for 144.0h; Step 2: 3-Amino-adamantane-1-carboxylic acid hydrochloride; To a 3-neck 5-L flask equipped with a reflux condenser, a mechanical stirrer and a temperature probe was added 3-acetylamino-adamantane-1-carboxylic acid (432 g, 1.82 mol), water (1.00 L) and concentrated hydrochloric acid (2.44 L), and the resulting mixture was heated at 95 C. for 6 days. During this time, solid material precipitated from the solution. After cooling at 0 C., the solids were filtered and washed with acetone. The solid was then dried under high vacuum at 50 C. for about 2 hours to afford 328 g (78%) of the title compound, 3-amino-adamantane-1-carboxylic acid hydrochloride, as a white solid. 1H NMR (300 MHz, DMSO-td6) delta 12.35 (br s, 1H), 8.27 (br s, 3H), 2.22-2.12 (m, 2H), 1.92-1.85 (m, 2H), 1.83-1.71 (ml 6H), 1.69-1.48 (m, 4H).
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