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METHYL 3-(4-HYDROXY-2-METHOXYPHENYL)PROPANOATE, also known as methyl rosmarinate, is a chemical compound found in various plants, particularly in the Rosmarinus officinalis (rosemary) species. It is recognized for its antioxidant properties, pleasant aromatic profile, and potential anti-inflammatory and antiproliferative effects, making it a valuable compound for use in food, cosmetic, and pharmaceutical industries.

628333-35-7

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628333-35-7 Usage

Uses

Used in Food Industry:
METHYL 3-(4-HYDROXY-2-METHOXYPHENYL)PROPANOATE is used as a natural antioxidant for enhancing the stability and shelf life of various food products, due to its ability to prevent oxidation and spoilage.
Used in Cosmetic Industry:
METHYL 3-(4-HYDROXY-2-METHOXYPHENYL)PROPANOATE is used as an antioxidant and aromatic ingredient in cosmetic products, providing both preservative and sensory benefits.
Used in Pharmaceutical Applications:
METHYL 3-(4-HYDROXY-2-METHOXYPHENYL)PROPANOATE is used as a potential anti-inflammatory and antiproliferative agent, making it a subject of interest for the development of new drugs and treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 628333-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,8,3,3 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 628333-35:
(8*6)+(7*2)+(6*8)+(5*3)+(4*3)+(3*3)+(2*3)+(1*5)=157
157 % 10 = 7
So 628333-35-7 is a valid CAS Registry Number.

628333-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(4-hydroxy-2-methoxyphenyl)propanoate

1.2 Other means of identification

Product number -
Other names -

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:628333-35-7 SDS

628333-35-7Downstream Products

628333-35-7Relevant academic research and scientific papers

Revisiting Arene C(sp2)?H Amidation by Intramolecular Transfer of Iridium Nitrenoids: Evidence for a Spirocyclization Pathway

Hwang, Yeongyu,Park, Yoonsu,Kim, Yeong Bum,Kim, Dongwook,Chang, Sukbok

supporting information, p. 13565 - 13569 (2018/09/25)

Two mechanistic pathways, that is, electrocyclization and electrophilic aromatic substitution, are operative in most intramolecular C?H amination reactions proceeding by metal nitrenoid catalysis. Reported here is an alternative mechanistic scaffold leading to benzofused δ-lactams selectively. Integrated experimental and computational analysis revealed that the reaction proceeds by a key spirocyclization step followed by a skeletal rearrangement. Based on this mechanistic insight, a new synthetic route to spirolactams has been developed.

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