Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C9H13NO |
| Molecular Weight | 151.2056 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N[C@H](CO)CC1=CC=CC=C1
InChI
InChIKey=STVVMTBJNDTZBF-VIFPVBQESA-N
InChI=1S/C9H13NO/c10-9(7-11)6-8-4-2-1-3-5-8/h1-5,9,11H,6-7,10H2/t9-/m0/s1
| Molecular Formula | C9H13NO |
| Molecular Weight | 151.2056 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Tuning and enhancing enantioselective quenching of calixarene hosts by chiral guest amines. | 2002 Jan 1 |
|
| Resolution of 1- and 2-naphthylmethoxyacetic acids, NMR reagents for absolute configuration determination, by use of L-phenylalaninol. | 2003 Aug |
|
| Chiral oxime ethers in asymmetric synthesis. O-(1-Phenylbutyl)benzyloxyacetaldoxime, a versatile reagent for the asymmetric synthesis of protected 1,2-aminoalcohols, alpha-amino acid derivatives, and 2-hydroxymethyl nitrogen heterocycles including iminosugars. | 2005 Apr 7 |
|
| New route to enantiopure MalphaNP acid, a powerful resolution and chiral 1H NMR anisotropy reagent. | 2007 May 15 |
|
| Synthesis of enantiopure 2-aryl-2-methoxypropionic acids and determination of their absolute configurations by X-ray crystallography. | 2008 Mar |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:29:32 UTC 2023
by
admin
on
Sat Dec 16 11:29:32 UTC 2023
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| Record UNII |
9GE9QOP0ET
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| Record Status |
Validated (UNII)
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| Record Version |
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447213
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3182-95-4
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DB04484
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221-674-4
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9GE9QOP0ET
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DTXSID001025528
Created by
admin on Sat Dec 16 11:29:32 UTC 2023 , Edited by admin on Sat Dec 16 11:29:32 UTC 2023
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| Related Record | Type | Details | ||
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ENANTIOMER -> ENANTIOMER |
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RACEMATE -> ENANTIOMER |
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