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(3,5-DIMETHOXY-4-HYDROXYPHENYL)ACETONE, also known as syringylacetone, is an organic compound derived from lignin, a complex organic polymer found in the cell walls of plants. It is characterized by its unique chemical structure, which includes two methoxy groups and a hydroxyl group attached to a phenyl ring, with an acetone group attached to the carbon at the para position. This structure endows it with various chemical and physical properties, making it a versatile compound for a range of applications.

19037-58-2

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19037-58-2 Usage

Uses

Used in Biomass Waste Treatment:
(3,5-DIMETHOXY-4-HYDROXYPHENYL)ACETONE is used as a chemical intermediate for the thermal decomposition of biomass wastes derived from palm oil production. Its unique structure allows it to break down complex organic materials into simpler compounds, facilitating the conversion of waste biomass into valuable products such as biofuels, chemicals, and materials.
Used in Chemical Synthesis:
(3,5-DIMETHOXY-4-HYDROXYPHENYL)ACETONE can be used as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its reactive functional groups enable it to participate in a wide range of chemical reactions, such as esterification, etherification, and condensation, making it a valuable starting material for the development of new molecules with specific properties and applications.
Used in Material Science:
(3,5-DIMETHOXY-4-HYDROXYPHENYL)ACETONE can be used as a component in the development of novel materials with unique properties, such as polymers, coatings, and adhesives. Its ability to form hydrogen bonds and participate in π-π interactions can contribute to the formation of supramolecular structures and improve the mechanical, thermal, and chemical properties of the resulting materials.
Used in Analytical Chemistry:
(3,5-DIMETHOXY-4-HYDROXYPHENYL)ACETONE can be employed as a reagent or a derivatization agent in analytical chemistry for the detection, identification, and quantification of various compounds. Its chromophoric properties and reactivity can be exploited to enhance the sensitivity and selectivity of analytical methods, such as high-performance liquid chromatography (HPLC), gas chromatography (GC), and mass spectrometry (MS).

Check Digit Verification of cas no

The CAS Registry Mumber 19037-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,3 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19037-58:
(7*1)+(6*9)+(5*0)+(4*3)+(3*7)+(2*5)+(1*8)=112
112 % 10 = 2
So 19037-58-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O4/c1-7(12)4-8-5-9(14-2)11(13)10(6-8)15-3/h5-6,13H,4H2,1-3H3

19037-58-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-hydroxy-3,5-dimethoxyphenyl)propan-2-one

1.2 Other means of identification

Product number -
Other names (4-hydroxy-3,5-dimethoxy-phenyl)-acetone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19037-58-2 SDS

19037-58-2Relevant academic research and scientific papers

Methoxyphenols from burning of Scandinavian forest plant materials

Kjaellstrand, Jennica,Ramnaes, Olle,Petersson, Goeran

, p. 735 - 741 (2007/10/03)

Semivolatile compounds in smoke from gram-scale incomplete burning of plant materials were assessed by gas chromatography and mass spectrometry. Gas syringe sampling was shown to be adequate by comparison with adsorbent sampling. Methoxyphenols as well as 1,6-anhydroglucose were released in amounts as large as 10 mg kg-1 of dry biomass at 90% combustion efficiency. Wood, twigs, bark and needles from the conifers Norway spruce and Scots pine emitted 12 reported 2-methoxyphenols in similar proportions. Grass, heather and birchwood released the same 2-methoxyphenols but also the corresponding 2,6-dimethoxyphenols which are characteristic of angiosperms. The methoxyphenols are formed from lignin and differ in structure by the group in para position relative to the phenolic OH group. Prominent phenols were those with trans-l-propenyl and ethenyl groups in that position. Vanillin, 4- hydroxy-3-methoxybenzaldehyde, was a prominent carbonyl compound from the conifer materials. (C) 2000 Elsevier Science Ltd.

Intramolecular Oxidative Coupling of Aromatic Compounds. V. para-para Diphenolic Oxidative Coupling as a Possible Route to the Eupodienone Skeleton

Carroll, Anthony R.,Krauss, Adrian S.,Taylor, Walter C.

, p. 277 - 292 (2007/10/02)

The synthesis of (2RS,3RS)-1,4-bis(4-hydroxy-3,5-dimethoxyphenyl)-2,3-dimethylbutan-1-one (9) is described.Diphenolic oxidative coupling of (9) gave the unstable dienone (24), which decomposed in methanol to give what is believed to be the acetal (26).Syn

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