Identification | More | [Name]
Methyl 3-(4-hydroxyphenyl)propionate | [CAS]
5597-50-2 | [Synonyms]
3-(4-HYDROXYPHENYL)PROPIONIC ACID METHYL ESTER 3-(4'-HYDROXYPHENYL)-PROPIONIC ACID-OME 3-(4-HYDROXY-PHENYL)-PROPIONIC ACID-OME 4-hydroxy-benzenepropanoic acid methyl ester METHYL 3-(4-HYDROXYPHENYL)PROPIONATE METHYL P-HYDROXYHYDROCINNAMATE 4-hydroxy-benzenepropanoicacimethylester Hydrocinnamic acid, p-hydroxy-, methyl ester Methyl 3-(4-hydroxyphenyl)propanoate Methyl 3-(p-hydroxyphenyl)propionate Methyl 4-hydroxyhydrocinnamate Propanoic acid, 3-(4-hydroxyphenyl), methyl ester 3-(4-hydroxybenzene)propionic methyl ester Methyl 4-hydroxyphenylpropionate METHYL 3-(4-HYDROXYPHENYL)PROPIONATE, 97 % 4-Hydroxyphenylpropionic Acid Methyl Ester 3-(4-HYDROCHLORIDE )PROPIONIC ACID METHYL ESTER Methyl p-hydroxyphenylpropionate 3-(4-Hydroxyphenyl)propanoic acid methyl ester 4-Hydroxybenzenepropionic acid methyl ester | [Molecular Formula]
C10H12O3 | [MDL Number]
MFCD00071577 | [Molecular Weight]
180.2 | [MOL File]
5597-50-2.mol |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [HS Code ]
29181990 |
Hazard Information | Back Directory | [Chemical Properties]
white transparent low melting mass | [Uses]
Methyl 3-(4-hydroxyphenyl)propionate may be used in the enzymatic coupling of saccharides to protein. | [Definition]
ChEBI: Methyl 3-(4-hydroxyphenyl)propionate is a methyl ester resulting from the formal condensation of the carboxy group of phloretic acid with methanol. It is a nitrification inhibitor and a plant growth regulator. It has a role as a nitrification inhibitor and a plant growth regulator. It is a member of phenols and a methyl ester. It is functionally related to a phloretic acid. | [General Description]
Methyl 3-(4-hydroxyphenyl)propionate is reported to be responsible for biological nitrification inhibition in sorghum (Sorghum bicolor). |
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