bromocinnamal
2-propenal, 2-bromo-3-phenyl-, (Z)-
Identification
| Name | bromocinnamal |
| IUPAC | (Z)-2-bromo-3-phenylprop-2-enal |
| CAS Number | 5443-49-2 |
| EINECS | 226-637-6 |
| FDA UNII | Search |
| Molecular Formula | C9 H7 Br O |
| Molecular Weight | 211.05799000 |
| MDL Number | MFCD00006965 |
| Nikkaji Number | J60.277I |
| Beilstein | 1099733 |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 304.44 °C. @ 760.00 mm Hg (est) |
| Vapor Pressure | 0.001000 mmHg @ 25.00 °C. (est) |
| Flash Point | 230.00 °F. TCC ( 110.20 °C. ) (est) |
| logP (o/w) | 2.491 (est) |
| Soluble in | water, 496 mg/L @ 25 °C (est) |
Cosmetic Information
| CosIng | cosmetic data |
| Cosmetic Uses | fragrance |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | intraperitoneal-mouse LD50 822 mg/kg |
| Dermal Toxicity | subcutaneous-mouse LD50 2200 mg/kg |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | cosmetic agents |
| Recommendation for bromocinnamal usage levels up to | not for fragrance use. |
| Recommendation for bromocinnamal flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
alphabrocine
(2Z)-2-
bromo-3-phenyl-2-propenal
(Z)-2-
bromo-3-phenyl-2-propenal
2-
bromo-3-phenyl-2-propenal
(2Z)-2-
bromo-3-phenylacrylaldehyde
(Z)-2-
bromo-3-phenylacrylaldehyde
2-
bromo-3-phenylacrylaldehyde
(2Z)-2-
bromo-3-phenylprop-2-enal
(Z)-2-
bromo-3-phenylprop-2-enal
a-
bromocinnamaldehyde
alpha-
bromocinnamaldehyde
a-
bromocinnamic aldehyde
cinnamaldehyde, a-bromo-
2-
propenal, 2-bromo-3-phenyl- (9CI)
2-
propenal, 2-bromo-3-phenyl-, (2Z)-
2-
propenal, 2-bromo-3-phenyl-, (Z)-
PubMed:
Masuda borylation-Suzuki coupling (MBSC) sequence of vinylhalides and its application in a one-pot synthesis of 3,4-biarylpyrazoles.
PubMed:
The comparison of α-bromo-4-chlorocinnamaldehyde and cinnamaldehyde on coxsackie virus B3-induced myocarditis and their mechanisms.
PubMed:
Synthesis, pharmacological activity and structure affinity relationships of spirocyclic Ï(1) receptor ligands with a (2-fluoroethyl) residue in 3-position.
PubMed:
Inhibition of chitin synthases and antifungal activities by 2'-benzoyloxycinnamaldehyde from Pleuropterus ciliinervis and its derivatives.
PubMed:
Guanidinium ylide mediated aziridination: identification of a spiro imidazolidine-oxazolidine intermediate.
PubMed:
Genotoxicity of 2-halocinnamaldehydes in two bacterial assays. Induction of SOS repair and frame-shift mutation.
PubMed:
[Combined long-term toxicity/carcinogenicity test of alpha-bromocinnamic aldehyde (BCA) applied to female mouse skin].
PubMed:
[Alpha-bromocinnamaldehyde, its mutagenicity and contents in commercial products].