Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H7Br |
| Molecular Weight | 207.067 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
BrC1=CC=C2C=CC=CC2=C1
InChI
InChIKey=APSMUYYLXZULMS-UHFFFAOYSA-N
InChI=1S/C10H7Br/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H
| Molecular Formula | C10H7Br |
| Molecular Weight | 207.067 |
| 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 evaluation of 1-(1-(Benzo[b]thiophen-2-yl)cyclohexyl)piperidine (BTCP) analogues as inhibitors of trypanothione reductase. | 2009-08 |
|
| Characterization of a modular enzyme of exo-1,5-alpha-L-arabinofuranosidase and arabinan binding module from Streptomyces avermitilis NBRC14893. | 2008-09 |
|
| Binary and ternary complexes containing alpha-cyclodextrin and bromonaphthalene derivatives: a note of caution in interpreting UV absorption spectral data. | 2006-11-16 |
|
| UVA photoirradiation of halogenated-polycyclic aromatic hydrocarbons leading to induction of lipid peroxidation. | 2006-06 |
|
| Mechanisms of dioxin formation from the high-temperature pyrolysis of 2-bromophenol. | 2003-12-15 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:15:50 GMT 2025
by
admin
on
Mon Mar 31 20:15:50 GMT 2025
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| Record UNII |
SYU33I753N
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| Record Status |
Validated (UNII)
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| Record Version |
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PRIMARY | Merck Index |