Details
Stereochemistry | RACEMIC |
Molecular Formula | C9H9ClN2O |
Molecular Weight | 196.634 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NCC(O1)C2=CC=C(Cl)C=C2
InChI
InChIKey=HAHOPPGVHWVBRR-UHFFFAOYSA-N
InChI=1S/C9H9ClN2O/c10-7-3-1-6(2-4-7)8-5-12-9(11)13-8/h1-4,8H,5H2,(H2,11,12)
Molecular Formula | C9H9ClN2O |
Molecular Weight | 196.634 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Originator
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:08:35 GMT 2023
by
admin
on
Fri Dec 15 15:08:35 GMT 2023
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Record UNII |
O1R2462WA0
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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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Systematic Name | English | ||
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Code | English | ||
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Common Name | English | ||
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Code | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29728
Created by
admin on Fri Dec 15 15:08:35 GMT 2023 , Edited by admin on Fri Dec 15 15:08:35 GMT 2023
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Code System | Code | Type | Description | ||
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100000084526
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19752
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CHEMBL2104179
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3876-10-6
Created by
admin on Fri Dec 15 15:08:35 GMT 2023 , Edited by admin on Fri Dec 15 15:08:35 GMT 2023
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1653
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admin on Fri Dec 15 15:08:35 GMT 2023 , Edited by admin on Fri Dec 15 15:08:35 GMT 2023
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139299
Created by
admin on Fri Dec 15 15:08:35 GMT 2023 , Edited by admin on Fri Dec 15 15:08:35 GMT 2023
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C72177
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admin on Fri Dec 15 15:08:35 GMT 2023 , Edited by admin on Fri Dec 15 15:08:35 GMT 2023
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SUB06724MIG
Created by
admin on Fri Dec 15 15:08:35 GMT 2023 , Edited by admin on Fri Dec 15 15:08:35 GMT 2023
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PRIMARY | |||
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DTXSID30863286
Created by
admin on Fri Dec 15 15:08:35 GMT 2023 , Edited by admin on Fri Dec 15 15:08:35 GMT 2023
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CLOMINOREX
Created by
admin on Fri Dec 15 15:08:35 GMT 2023 , Edited by admin on Fri Dec 15 15:08:35 GMT 2023
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O1R2462WA0
Created by
admin on Fri Dec 15 15:08:35 GMT 2023 , Edited by admin on Fri Dec 15 15:08:35 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 |