Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H6Br2 |
| Molecular Weight | 249.931 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
BrCC1=CC=C(Br)C=C1
InChI
InChIKey=YLRBJYMANQKEAW-UHFFFAOYSA-N
InChI=1S/C7H6Br2/c8-5-6-1-3-7(9)4-2-6/h1-4H,5H2
| Molecular Formula | C7H6Br2 |
| Molecular Weight | 249.931 |
| 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 |
|---|---|---|
| Synthesis and PET studies of [(11)C-cyano]letrozole (Femara), an aromatase inhibitor drug. | 2009-02 |
|
| 3,6-Dibromo-9-(4-bromo-benz-yl)-9H-carbazole. | 2009-01-08 |
|
| Distributed Drug Discovery, Part 2: global rehearsal of alkylating agents for the synthesis of resin-bound unnatural amino acids and virtual D(3) catalog construction. | 2008-12-25 |
|
| Distributed Drug Discovery, Part 3: using D(3) methodology to synthesize analogs of an anti-melanoma compound. | 2008-12-25 |
|
| Solution-phase synthesis of an aminomethyl-substituted biaryl library via sequential amine N-alkylation and Suzuki cross-coupling. | 2001-09-11 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:21:50 GMT 2025
by
admin
on
Mon Mar 31 21:21:50 GMT 2025
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| Record UNII |
3D1TTL8BGN
|
| Record Status |
Validated (UNII)
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| Record Version |
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