Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H11NO2 |
| Molecular Weight | 177.1998 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)[C@H]1CC2=CC=CC=C2CN1
InChI
InChIKey=BWKMGYQJPOAASG-SECBINFHSA-N
InChI=1S/C10H11NO2/c12-10(13)9-5-7-3-1-2-4-8(7)6-11-9/h1-4,9,11H,5-6H2,(H,12,13)/t9-/m1/s1
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/?term=1335996 | http://www.sigmaaldrich.com/catalog/product/aldrich/87433?lang=en®ion=USDOI: 10.1007/BF02261393
Sources: https://www.ncbi.nlm.nih.gov/pubmed/?term=1335996 | http://www.sigmaaldrich.com/catalog/product/aldrich/87433?lang=en®ion=USDOI: 10.1007/BF02261393
Racemic alpha-alkyl-alpha-amino-acids are difficult solutes to resolve on chiral chromatographic phases derived from proline or pipecolic acid-polyacrylamide. The use of L-3-carboxy-1,2,3,4-tetrahydroisoquinoline (L-porretine) as the chiral selector instead of the former alpha-amino-acids selectively resolves the alpha-alkyl-alpha-amino-acids.
Originator
Approval Year
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712398
Created by
admin on Sat Dec 16 14:59:04 GMT 2023 , Edited by admin on Sat Dec 16 14:59:04 GMT 2023
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103733-65-9
Created by
admin on Sat Dec 16 14:59:04 GMT 2023 , Edited by admin on Sat Dec 16 14:59:04 GMT 2023
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30WOC9CAC6
Created by
admin on Sat Dec 16 14:59:04 GMT 2023 , Edited by admin on Sat Dec 16 14:59:04 GMT 2023
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SUBSTANCE RECORD
