Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C9H13NO2.C4H6O6 |
Molecular Weight | 317.2919 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O[C@H]([C@@H](O)C(O)=O)C(O)=O.CNC[C@H](O)C1=CC=CC(O)=C1
InChI
InChIKey=NHKOTKKHHYKARN-NDAAPVSOSA-N
InChI=1S/C9H13NO2.C4H6O6/c1-10-6-9(12)7-3-2-4-8(11)5-7;5-1(3(7)8)2(6)4(9)10/h2-5,9-12H,6H2,1H3;1-2,5-6H,(H,7,8)(H,9,10)/t9-;1-,2-/m01/s1
Molecular Formula | C9H13NO2 |
Molecular Weight | 167.205 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Molecular Formula | C4H6O6 |
Molecular Weight | 150.0868 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 05:15:32 UTC 2023
by
admin
on
Sat Dec 16 05:15:32 UTC 2023
|
Record UNII |
27O3Q5ML57
|
Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29709
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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CFR |
21 CFR 341.20
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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Code System | Code | Type | Description | ||
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27O3Q5ML57
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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PRIMARY | |||
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14787-58-7
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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NON-SPECIFIC STOICHIOMETRY | |||
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27O3Q5ML57
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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PRIMARY | |||
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91167
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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PRIMARY | RxNorm | ||
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CHEMBL1215
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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PRIMARY | |||
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C66378
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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PRIMARY | |||
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DTXSID901026092
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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100000085297
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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DBSALT001320
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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241-219-3
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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PRIMARY | |||
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SUB03775MIG
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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1532950
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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PRIMARY | |||
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17162-39-9
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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46174134
Created by
admin on Sat Dec 16 05:15:33 UTC 2023 , Edited by admin on Sat Dec 16 05:15:33 UTC 2023
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PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
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PARENT -> SALT/SOLVATE | |||
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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
---|---|---|---|---|
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |