CAS 7159-96-8

Ethyl 3-hydroxyphenylcarbamate

Description:

Ethyl 3-hydroxyphenylcarbamate, with the CAS number 7159-96-8, is an organic compound characterized by its carbamate functional group and a phenolic structure. It typically appears as a white to off-white solid or crystalline powder. This compound is known for its potential applications in pharmaceuticals and agrochemicals, often serving as an intermediate in the synthesis of various bioactive molecules. Ethyl 3-hydroxyphenylcarbamate exhibits moderate solubility in organic solvents, while its solubility in water may vary depending on pH and temperature. The presence of the hydroxy group contributes to its reactivity and ability to form hydrogen bonds, influencing its biological activity and interactions with other substances. Additionally, this compound may possess antioxidant properties, making it of interest in research related to health and disease prevention. As with many chemical substances, proper handling and safety precautions are essential due to potential toxicity or environmental impact.

Formula: C₉H₁₁NO₃

InChI: InChI=1/C9H11NO3/c1-2-13-9(12)10-7-4-3-5-8(11)6-7/h3-6,11H,2H2,1H3,(H,10,12)

InChI key: InChIKey=KCLZXXMMEDEBMF-UHFFFAOYSA-N

SMILES: N(C(OCC)=O)C1=CC(O)=CC=C1

Synonyms:

• (3-Hydroxy-Phenyl)-Carbamic Acid Ethyl Ester
• (3-Hydroxyphenyl)carbamic acid ethyl ester
• 3-(Ethoxycarbonylamino)phenol
• 3-Carbethoxyaminophenol
• 3-Ethyloxycarbonylaminophenol
• Carbamic acid, (3-hydroxyphenyl)-, ethyl ester
• Carbamic acid, N-(3-hydroxyphenyl)-, ethyl ester
• Carbanilic acid, m-hydroxy-, ethyl ester
• Carbanilic acid, m-hydroxy-, ethyl esters
• Ethyl (m-hydroxyphenyl)carbamate
• Ethyl 3-hydroxycarbanilate
• Ethyl 3-hydroxyphenylcarbamate
• Ethyl N-(3-hydroxyphenyl)carbamate
• NSC 222551
• m-(Ethoxycarbonylamino)phenol
• Ethyl (3-hydroxyphenyl)carbamate
• Ethyl-3-hydroxyphenolcarbamate
• (3-hydroxyphenyl)-carbamicaciethylester
• ethyln-(3-hydroxyphenyl)carbamate
• ethylm-hydroxycarbanilate
• N-(3-Hydroxyphenyl)carbamic acid ethyl ester
• (3-Hydroxy-Phenyl)-carbanicacid ethyl ester
• m-hydroxy-carbanilicaciethylester
• ethyl3-hydroxycarbanilate
• AKOS BBS-00008072

Ethyl (3-Hydroxyphenyl)carbamate

CAS: 7159-96-8

Formula: C₉H₁₁NO₃

Purity: >97.0%(GC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 181.19

Ref: 3B-E1227

Ethyl (3-hydroxyphenyl)carbamate

CAS: 7159-96-8

Formula: C₉H₁₁NO₃

Purity: %

Color and Shape: Solid

Molecular weight: 181.1885

Ref: IN-DA0064T9

Ethyl 3-Hydroxyphenylcarbamate

CAS: 7159-96-8

Ethyl 3-Hydroxyphenylcarbamate

Purity: 99%

Molecular weight: 181.18854g/mol

Ref: 54-OR1027550

Ethyl (3-hydroxyphenyl)carbamate

CAS: 7159-96-8

Ethyl (3-hydroxyphenyl)carbamate is a bioactive chemical.

Formula: C₉H₁₁NO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 181.19

Ref: TM-T21203

Ethyl (3-hydroxyphenyl)carbamate

CAS: 7159-96-8

Formula: C₉H₁₁NO₃

Purity: 95+%

Color and Shape: Solid

Molecular weight: 181.191

Ref: 10-F329531

Ethyl (3-Hydroxyphenyl)carbamate

CAS: 7159-96-8

Ethyl (3-Hydroxyphenyl)carbamate is a carbonyl group that is produced by the hydrolysis of triticum aestivum. This product has been shown to have a synergistic interaction with retroflexus and bioassay, an imaging technique used to measure the photosynthetic activity of plants. Ethyl (3-Hydroxyphenyl)carbamate has low light fluorescence properties, which are useful for the detection of sugarbeet in low light conditions. The symptoms of ethyl (3-hydroxyphenyl)carbamate exposure include a constant and acceptor, which is a molecule or atom that accepts electrons from an electron donor in chemical reactions. Ethyl (3-hydroxyphenyl)carbamate can react with proton to form arvensis, a sugar found in sugarbeets.

Formula: C₉H₁₁NO₃

Purity: Min. 95%

Molecular weight: 181.19 g/mol

Ref: 3D-HAA15996