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| 2,6,6-TRIMETHYL-1-CYCLOHEXENE-1-ACETALDEHYDE Basic information |
| Product Name: | 2,6,6-TRIMETHYL-1-CYCLOHEXENE-1-ACETALDEHYDE | | Synonyms: | (2,6,6-Trimethyl-1-cyclohexen-1-yl)acetaldehyde;2,6,6-trimethyl-1-cyclohexene-1-acetaldehyd;B-HOMOCYCLOCITRAL;FEMA 3474;2,6,6-TRIMETHYL-1-CYCLOHEXEN-1-ACETALDEHYDE;2,6,6-TRIMETHYL-1-CYCLOHEXENE-1-ACETALDEHYDE;2-(2,6,6-triMethylcyclohex-1-en-1-yl)acetaldehyde;2,6,6-Trimethyl-1-cyclohexene-1-acetaldehyde technical grade, 80% | | CAS: | 472-66-2 | | MF: | C11H18O | | MW: | 166.26 | | EINECS: | 207-454-0 | | Product Categories: | Aldehydes;Building Blocks;C10-C12;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks | | Mol File: | 472-66-2.mol |
| 2,6,6-TRIMETHYL-1-CYCLOHEXENE-1-ACETALDEHYDE Chemical Properties |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 |
| 2,6,6-TRIMETHYL-1-CYCLOHEXENE-1-ACETALDEHYDE Usage And Synthesis |
| Uses | 2,6,6-Trimethyl-1-cyclohexene-1-acetaldehyde can be used as a starting material to prepare: - (±)-Aeginetolide by oxidation in the presence of meta-chloroperoxybenzoic acid (m-CPBA).
- (±)-Dihydroactinidiolide (a C11-terpenic lactone) via dehydration of key intermediate aeginetolide.
It can also be used as a key intermediate to synthesize drimane-related sesquiterpenes and substituted retinoic acid analogs. | | Taste threshold values | Taste characteristics at 15 ppm: cooling, woody, oily, soapy, citrus with a berry, orris-like nuance. |
| 2,6,6-TRIMETHYL-1-CYCLOHEXENE-1-ACETALDEHYDE Preparation Products And Raw materials |
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