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17702-88-4

17702-88-4 Structure

17702-88-4 Structure
IdentificationBack Directory
[Name]

2-AMINOCAPRIC ACID
[CAS]

17702-88-4
[Synonyms]

DL-decyline [
2-AMINOCAPRIC ACID
2-AMINODECANOIC ACID
D-2-Aminocapric acid
REF DUPL: DL-decyline
Decanoic acid, 2-amino-
2-Aminodecanoicacidpurum
(-)-D-2-Aminocapric acid
(R)-2-Aminodecanoic acid
D,L 2-AMINODECANOIC ACID
[R,(-)]-2-Aminocapric acid
[R,(-)]-2-Aminodecanoic acid
2-AMINODECANOIC ACID PURUM 97%
DL-decyline 2-AMinodecanoic acid
[Molecular Formula]

C10H21NO2
[MDL Number]

MFCD01862887
[MOL File]

17702-88-4.mol
[Molecular Weight]

187.28
Chemical PropertiesBack Directory
[Melting point ]

~262 °C (dec.)
[Boiling point ]

300.9±25.0 °C(Predicted)
[density ]

0.973±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

2.55±0.24(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[WGK Germany ]

3
Hazard InformationBack Directory
[Synthesis]

sodium:cyanide

773837-37-9

1-Nonanal

124-19-6

2-AMINOCAPRIC ACID

17702-88-4

GENERAL METHOD: Acetylacetonate dicarbonylrhodium (Rh(acac)(CO)2, 2.6 mg, 0.01 mmol) and xantphos (28.9 mg, 0.05 mmol) were placed in an autoclave according to the typical method described above. Subsequently, a solution of 1,2-dimethoxyethane (DME, 8 mL) of olefin (5 mmol) was added through a cannula. The autoclave was pressurized with a 20 bar carbon monoxide/hydrogen (1:1 molar ratio) mixture and the reaction was stirred for 18 h at 80 °C. Upon completion of the reaction, the reactor was cooled to room temperature, an aqueous solution (2 mL) of ammonium chloride (NH4Cl, 5.5 mmol) and sodium cyanide (NaCN, 5.5 mmol) was added through the inlet cannula, and the reaction was continued for another 20 hours at 50 °C. After post-processing and purification, the resulting α-aminonitrile (4.1 mmol) was suspended in concentrated hydrochloric acid solution and stirred at 40 °C for 6 h. The product was then dissolved in methanol. The product was dissolved in methanol and the solvent was evaporated after adjusting the pH to the isoelectric point with ammonia (aq) to finally obtain the target amino acid 2-aminodecanoic acid.

[References]

[1] Tetrahedron, 2017, vol. 73, # 17, p. 2389 - 2395
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