Name | Value |
---|---|
Natural Product | |
InChI=1S/C10H12N2O3/c11-7-4-2-1-3-6(7)9(13)5-8(12)10(14)15/h1-4,8H,5,11-12H2,(H,14,15)/t8-/m0/s1 | |
YGPSJZOEDVAXAB-QMMMGPOBSA-N | |
C10H12N2O3 | |
208.08479224399997 | |
O=C(O)C(N)CC(=O)C=1C=CC=CC1N |
External Identifier | Value |
---|---|
2922-83-0 | |
16946 | |
141580 | |
C00328 | |
161166 6971029 |
Name | Value |
---|---|
OUF00313 | |
2016.01.19 (Created 2010.05.20, modified 2013.04.24) | |
Tsujimoto Y, Tsugawa H, Bamba T, Fukusaki E, engineering department, Osaka Univ. | |
CC BY-SA | |
The chemical compound was chemically modified with N-methyl-N-trimethylsilyl-trifluoroacetamide (MSTFA) before GC-MS analysis. When it has two or more functional groups, this modification gave a mixture of the TMS derivatives having different number of TMS groups at different functional groups. | |
208.08479 | |
Pegasus III TOF-MS system, Leco; GC 6890, Agilent Technologies | |
GC-EI-TOF | |
MS1 | |
1 ml/min | |
200 C | |
85-500 | |
CP-SIL 8 CB LOW BLEED/MS | |
230 C | |
80 C (Duration 2 min)-330 C (rate: 15 C/min; Duration 6 min) | |
2187.101 | |
841.093 sec | |
250 C | |
ChromaTOF ver. 2.32 (LECO) | |
positive | |
4.204737820474912 | |
0.7671984743543261 |