3',4',5'-trimethoxyacetophenone

ethanone, 1-(3,4,5-trimethoxyphenyl)- (9CI)

CAS: 1136-86-3 C11 H14 O4 MW: 210.22938000

Identification

Name3',4',5'-trimethoxyacetophenone
CAS Number1136-86-3
EINECS214-501-9
FDA UNII35KU75558G
Molecular FormulaC11 H14 O4
Molecular Weight210.22938000
MDL NumberMFCD00008738
Nikkaji NumberJ150.377D
Beilstein1463133

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Soluble in water, 3772 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryinformation only not used for fragrances or flavors
Recommendation for 3',4',5'-trimethoxyacetophenone usage levels up tonot for fragrance use.
Recommendation for 3',4',5'-trimethoxyacetophenone flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

mitracarpus scaber ocotea comoriensis bark pequena enana proiphys amboinensis

Synonyms

ethanone, 1-(3,4,5-trimethoxyphenyl)- (9CI) (3,4,5- trimethoxy)acetophenone 1-(3,4,5- trimethoxyphenyl)ethanone PubMed: Atropa belladonna hairy roots: orchestration of concurrent oxidation and reduction reactions for biotransformation of carbonyl compounds. PubMed: The mechanism of tubulin-colchicine recognition--a kinetic study of the binding of a bicyclic colchicine analogue with a minor modification of the A ring. PubMed: Evidence for an alternative pathway for colchicine binding to tubulin, based on the binding kinetics of the constituent rings. PubMed: Fluorescence stopped-flow study of the interaction of tubulin with the antimitotic drug MDL 27048.