Weight | 196.202 g/mol |
---|---|
Formula | C10H12O4 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 4 |
3,4,5-TRIMETHOXYBENZALDEHYDE (86-81-7)
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- An Efficient Synthesis of 3,4,5-Trimethoxybenzaldehyde from Vanillin (Synthesis, 1983)
- Synthesis of 3,4,5-Trimethoxybenzaldehyde (Synthetic Communications, 1990)
- Regioselective reductive electrophilic substitution of derivatives of 3,4,5-trimethoxybenzaldehyde (Journal of Organic Chemistry, 1992)
- The selective liquid-phase oxidation of 3,4,5-trimethoxytoluene to 3,4,5-trimethoxybenzaldehyde (Bulletin of the Chemical Society of Japan, 1988)
- Synthetic routes to 3,4,5-trimethoxybenzaldehyde (review) (Pharmaceutical Chemistry Journal, 1990)
- Efficient synthesis of 3,4,5-trimethoxybenzaldehyde via Reissert aldehyde synthesis (Journal of Organic Chemistry, 1982)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=CC(=CC(=C1OC)OC)C=O
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InChIKeyOPHQOIGEOHXOGX-UHFFFAOYSA-N
- Pubchem - 3,4,5-TRIMETHOXYBENZALDEHYDE
- Wikipedia - 3,4,5-trimethoxybenzaldehyde
3,4,5-Trimethoxybenzaldehyde is an organic compound. Within this class of compounds the chemical is categorized as a trisubstituted aromatic aldehyde.
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Similar Compounds
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3,4-Dihydroxy-5-methoxybenzaldehyde
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3,4-Dimethoxybenzaldehyde
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Vanillin
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2,4,5-TRIMETHOXYBENZALDEHYDE
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(4-formyl-2,6-dimethoxyphenoxy)acetic acid
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3,4,5-Trimethoxybenzyl alcohol
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4-(allyloxy)-3-methoxybenzaldehyde
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3,5-Dimethoxybenzaldehyde
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4-isopropoxy-3-methoxybenzaldehyde
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3-ALLYLOXY-4-METHOXYBENZALDEHYDE
(18075-40-6)
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4-(allyloxy)-3-ethoxybenzaldehyde
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342592-62-5
(342592-62-5)
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3,4,5-Trimethoxybenzylamine
(18638-99-8)
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3,4,5-Triethoxybenzoic acid
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3-Isopropoxy-4-methoxybenzaldehyde
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3',4'-Dimethoxyacetophenone
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3,4,5-Trimethoxybenzyl chloride
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428847-37-4
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Methyl 3,4,5-trimethoxybenzoate
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3,4,5-Trimethoxybenzohydrazide
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4-isobutoxy-3-methoxybenzaldehyde
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Propioveratrone
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3,4-Diethoxybenzoic acid
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