Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C14H14O2 |
| Molecular Weight | 214.2598 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O[C@H]([C@@H](O)C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=IHPDTPWNFBQHEB-KBPBESRZSA-N
InChI=1S/C14H14O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13-16H/t13-,14-/m0/s1
| Molecular Formula | C14H14O2 |
| Molecular Weight | 214.2598 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Chiral separation of enantiomeric 1,2-diamines using molecular imprinting method and selectivity enhancement by addition of achiral primary amines into eluents. | 2002 Jan |
|
| Synthesis of (+)-polyoxamic acid and D-sorbitol from simple achiral allylic halides employing (S,S)-hydrobenzoin as a chiral source. | 2002 May 21 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:32:46 GMT 2023
by
admin
on
Sat Dec 16 09:32:46 GMT 2023
|
| Record UNII |
WX45Q7714B
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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DTXSID00357389
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853020
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2325-10-2
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WX45Q7714B
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admin on Sat Dec 16 09:32:46 GMT 2023 , Edited by admin on Sat Dec 16 09:32:46 GMT 2023
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m6085
Created by
admin on Sat Dec 16 09:32:46 GMT 2023 , Edited by admin on Sat Dec 16 09:32:46 GMT 2023
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PRIMARY | Merck Index |