Details
Stereochemistry | RACEMIC |
Molecular Formula | C10H10Cl3NO3 |
Molecular Weight | 298.55 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)NC1=CC=C(OC(O)C(Cl)(Cl)Cl)C=C1
InChI
InChIKey=NFZJQAPVHJPJMD-UHFFFAOYSA-N
InChI=1S/C10H10Cl3NO3/c1-6(15)14-7-2-4-8(5-3-7)17-9(16)10(11,12)13/h2-5,9,16H,1H3,(H,14,15)
Molecular Formula | C10H10Cl3NO3 |
Molecular Weight | 298.55 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:26:44 GMT 2023
by
admin
on
Fri Dec 15 17:26:44 GMT 2023
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Record UNII |
41Z22TQD48
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Record Status |
Validated (UNII)
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Record Version |
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-
Download
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Official Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C241
Created by
admin on Fri Dec 15 17:26:44 GMT 2023 , Edited by admin on Fri Dec 15 17:26:44 GMT 2023
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Code System | Code | Type | Description | ||
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SUB06749MIG
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CHEMBL2104601
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100000084022
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admin on Fri Dec 15 17:26:44 GMT 2023 , Edited by admin on Fri Dec 15 17:26:44 GMT 2023
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239-776-2
Created by
admin on Fri Dec 15 17:26:44 GMT 2023 , Edited by admin on Fri Dec 15 17:26:44 GMT 2023
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41Z22TQD48
Created by
admin on Fri Dec 15 17:26:44 GMT 2023 , Edited by admin on Fri Dec 15 17:26:44 GMT 2023
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15687-05-5
Created by
admin on Fri Dec 15 17:26:44 GMT 2023 , Edited by admin on Fri Dec 15 17:26:44 GMT 2023
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71685
Created by
admin on Fri Dec 15 17:26:44 GMT 2023 , Edited by admin on Fri Dec 15 17:26:44 GMT 2023
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2130
Created by
admin on Fri Dec 15 17:26:44 GMT 2023 , Edited by admin on Fri Dec 15 17:26:44 GMT 2023
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C81380
Created by
admin on Fri Dec 15 17:26:44 GMT 2023 , Edited by admin on Fri Dec 15 17:26:44 GMT 2023
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DTXSID20864621
Created by
admin on Fri Dec 15 17:26:44 GMT 2023 , Edited by admin on Fri Dec 15 17:26:44 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |