Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H8O |
| Molecular Weight | 96.1271 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 2 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C\C=C\C=C\C=O
InChI
InChIKey=BATOPAZDIZEVQF-MQQKCMAXSA-N
InChI=1S/C6H8O/c1-2-3-4-5-6-7/h2-6H,1H3/b3-2+,5-4+
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Population-based in vitro hazard and concentration-response assessment of chemicals: the 1000 genomes high-throughput screening study. | 2015-05 |
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| Chemicals inducing acute irritant contact dermatitis mobilize intracellular calcium in human keratinocytes. | 2013-02 |
|
| Human aldo-keto reductases 1B1 and 1B10: a comparative study on their enzyme activity toward electrophilic carbonyl compounds. | 2011-05-30 |
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| NTP toxicology and carcinogensis Studies of 2,4-hexadienal (89% trans,trans isomer, CAS No. 142-83-6; 11% cis,trans isomer) (Gavage Studies). | 2003-10 |
|
| Structural and kinetic determinants of aldehyde reduction by aldose reductase. | 1999-01-05 |
Patents
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205-564-3
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82334
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1166
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7239
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878K4I6N7T
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16184
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142-83-6
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DTXSID2025391
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80466-34-8
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68096
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637564
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SUBSTANCE RECORD