Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H6Cl2 |
| Molecular Weight | 161.029 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(Cl)C=C1Cl
InChI
InChIKey=FUNUTBJJKQIVSY-UHFFFAOYSA-N
InChI=1S/C7H6Cl2/c1-5-2-3-6(8)4-7(5)9/h2-4H,1H3
| Molecular Formula | C7H6Cl2 |
| Molecular Weight | 161.029 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Rapid and selective catalytic oxidation of secondary alcohols at room temperature by using (N-heterocyclic carbene)-ni(0) systems. | 2010-06-18 |
|
| Discovery of 4-amino-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamides as selective, orally active inhibitors of protein kinase B (Akt). | 2010-03-11 |
|
| Synthesis, cannabinoid receptor affinity, molecular modeling studies and in vivo pharmacological evaluation of new substituted 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides. 2. Effect of the 3-carboxamide substituent on the affinity and selectivity profile. | 2009-08-01 |
|
| Diethyl 2,6-(2,4-dichloro-phen-yl)-4,8-dioxo-2,3,6,7-tetra-hydro-1H,5H-2,3a,4a,6,7a,8a-hexa-azacyclo-penta-[def]fluorene-8b,8c-dicarboxyl-ate. | 2009-03-06 |
|
| Redox-active dinitrodiphenylthioethers against Leishmania: synthesis, structure-activity relationships and mechanism of action studies. | 2009-01-15 |
|
| Probing the active site tightness of DNA polymerase in subangstrom increments. | 2005-11-01 |
|
| A series of nonpolar thymidine analogues of increasing size: DNA base pairing and stacking properties. | 2005-03-18 |
|
| Simultaneous toxicity and nutrient removals in simulated DEPHANOX (anaerobic/anoxic/oxic sequentials) process treating dinitrotoluene and trichlorotoluene. | 2004 |
|
| Metabolism of dichloromethylcatechols as central intermediates in the degradation of dichlorotoluenes by Ralstonia sp. strain PS12. | 2002-10 |
|
| Antimicrobial activity of 5-arylidene aromatic derivatives of hydantoin. Part 2. | 2002-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:07:14 GMT 2025
by
admin
on
Mon Mar 31 21:07:14 GMT 2025
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| Record UNII |
3S32N6LG3X
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| Record Status |
Validated (UNII)
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| Record Version |
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