Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H11Br |
| Molecular Weight | 199.088 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
BrCCCC1=CC=CC=C1
InChI
InChIKey=XMZQWZJMTBCUFT-UHFFFAOYSA-N
InChI=1S/C9H11Br/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6H,4,7-8H2
| Molecular Formula | C9H11Br |
| Molecular Weight | 199.088 |
| 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 |
|---|---|---|
| Improved tricyclic inhibitors of trypanothione reductase by screening and chemical synthesis. | 2009-08 |
|
| Synthesis of symmetrical organic carbonates via significantly enhanced alkylation of metal carbonates with alkyl halides/sulfonates in ionic liquid. | 2005-12-23 |
|
| Room-temperature Negishi cross-coupling of unactivated alkyl bromides with alkyl organozinc reagents utilizing a Pd/N-heterocyclic carbene catalyst. | 2005-10-14 |
|
| Mono- and dialkylations of pyrrole at C2 and C5 positions by nucleophilic substitution reaction in ionic liquid. | 2005-03-31 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:02:56 GMT 2025
by
admin
on
Mon Mar 31 19:02:56 GMT 2025
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| Record UNII |
6VX623QN9V
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| Record Status |
Validated (UNII)
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