Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C5H13NO.ClH |
Molecular Weight | 139.624 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(C)[C@H](N)CO
InChI
InChIKey=CYONGLLQMUYOPP-NUBCRITNSA-N
InChI=1S/C5H13NO.ClH/c1-4(2)5(6)3-7;/h4-5,7H,3,6H2,1-2H3;1H/t5-;/m1./s1
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C5H13NO |
Molecular Weight | 103.1628 |
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 |
---|---|---|
Sequences of polypeptide antibiotics stilboflavins, natural peptaibol libraries of the mold Stilbella flavipes. | 2001 Aug |
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A total synthesis of (-)-hemiasterlin using N-Bts methodology. | 2001 Nov 2 |
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Invariom-model refinement of L-valinol. | 2006 Nov |
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Molecular modeling of chiral-modified zeolite HY employed in enantioselective separation. | 2007 Jun |
|
Enantioseparation of phenylglycinol in chiral-modified zeolite HY: a molecular simulation study. | 2007 Jun |
|
Asymmetric synthesis of 8-aminoindolizidine from chiral 2-pyrroleimines. | 2008 Nov 7 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 19:20:41 GMT 2023
by
admin
on
Sat Dec 16 19:20:41 GMT 2023
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Record UNII |
CSD9XWZ26Q
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Record Status |
Validated (UNII)
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Record Version |
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17016-89-6
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DTXSID20647395
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24802562
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CSD9XWZ26Q
Created by
admin on Sat Dec 16 19:20:42 GMT 2023 , Edited by admin on Sat Dec 16 19:20:42 GMT 2023
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