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PHENYL 2-HYDROXY-4,5-DIMETHOXYBENZOATE is an organic compound classified as a benzoate ester. It is characterized by its white crystalline powder form and is recognized for its multifaceted applications across various industries due to its unique properties, including its potential as an antioxidant and anti-inflammatory agent.

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  • 877997-98-3 Structure
  • Basic information

    1. Product Name: PHENYL 2-HYDROXY-4,5-DIMETHOXYBENZOATE
    2. Synonyms: Benzoic acid,2-hydroxy-4,5-dimethoxy-,phenyl ester (for Acotiamide);Benzoic acid,2-hydroxy-4,5-dimethoxy-,phenyl ester;Ethyl 2-(2-hydroxy-4,5-diMethoxybenzaMido)thiazole-4-carboxylate;PHENYL 2-HYDROXY-4,5-DIMETHOXYBENZOATE;2-Hydroxy-4,5-dimethoxybenzoic acid phenyl ester;Phenyl 2-hydroxy-4,5-dimethoxybenzoate Benzoic acid,2-hydroxy-4,5-dimethoxy-,phenyl ester (for Acotiamide)
    3. CAS NO:877997-98-3
    4. Molecular Formula: C15H14O5
    5. Molecular Weight: 274.27
    6. EINECS: 1806241-263-5
    7. Product Categories: N/A
    8. Mol File: 877997-98-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 431.2±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.250±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 8.83±0.23(Predicted)
    10. CAS DataBase Reference: PHENYL 2-HYDROXY-4,5-DIMETHOXYBENZOATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: PHENYL 2-HYDROXY-4,5-DIMETHOXYBENZOATE(877997-98-3)
    12. EPA Substance Registry System: PHENYL 2-HYDROXY-4,5-DIMETHOXYBENZOATE(877997-98-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 877997-98-3(Hazardous Substances Data)

877997-98-3 Usage

Uses

Used in Cosmetic and Personal Care Industry:
PHENYL 2-HYDROXY-4,5-DIMETHOXYBENZOATE is used as a fragrance ingredient and a component in the formulation of cosmetic and personal care products, leveraging its antioxidant and anti-inflammatory properties to enhance product efficacy and safety.
Used in Food and Beverage Industry:
In the food and beverage sector, PHENYL 2-HYDROXY-4,5-DIMETHOXYBENZOATE serves as a flavoring agent, contributing to the taste and aroma profiles of various products while also potentially offering health benefits due to its antioxidant properties.
Used in Sunscreen Products:
PHENYL 2-HYDROXY-4,5-DIMETHOXYBENZOATE is utilized as a UV filter in sunscreen products, providing protection against harmful ultraviolet radiation and helping to prevent skin damage.

Check Digit Verification of cas no

The CAS Registry Mumber 877997-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,9,9 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 877997-98:
(8*8)+(7*7)+(6*7)+(5*9)+(4*9)+(3*7)+(2*9)+(1*8)=283
283 % 10 = 3
So 877997-98-3 is a valid CAS Registry Number.

877997-98-3SDS

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 PHENYL 2-HYDROXY-4,5-DIMETHOXYBENZOATE

1.2 Other means of identification

Product number -
Other names 2-hydroxy-4,5-dimethoxybenzoic acid phenyl ester

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:877997-98-3 SDS

877997-98-3Relevant articles and documents

arab League tests for the amine and a method for the preparation of its hydrochloride (by machine translation)

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Paragraph 0016, (2016/10/17)

The invention discloses a arab League tests for the amine method for preparing and its hydrochloride, 2 - [(2-hydroxy -4,5-dimethoxy-benzoyl) amino] - 1,3-thiazole-4-carboxylic acid methyl ester, and N, N-diisopropyl ethylenediamin in the molten state after reaction under N-[ 2 - (diisopropyl amino) ethyl] - 2 - [(2-hydroxy -4,5-dimethoxy-benzoyl) amino] - 1,3-thiazole-4-carboxamide, hydrochloric acid for hydrochloric acid prepared by adding dropwisely added methanol trihydrate arab League takes a test for somebody else the amine, the technical proposal of the present invention reduces the use of toluene, economic and convenient, the reaction is complete, process safety; reduced at the same time the residual toluene in the final product, and impurity 2 - [(2-hydroxy -4,5-dimethoxy-benzoyl) amino] - 4-carboxyl -1, the content of 3-thiazole, the product quality is promoted; and is easy to be refined and purification of the crude product, the reaction yield is high. (by machine translation)

METHOD FOR PRODUCING 2-BROMO-4,5-DIALKOXY BENZOIC ACID

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Paragraph 0039, (2013/10/07)

Provided is a method for effectively producing a 4,5-dialkoxy-2-hydroxybenzoic acid from an inexpensive raw material. A method for producing a 2-bromo-4,5-dialkoxybenzoic acid represented by the following formula (2): (wherein each of R1 and R2 represents a lower alkyl group), the method including causing a 3,4-dialkoxybenzoic acid represented by the following formula (1): (wherein R1 and R2 have the same meanings as defined above) to react with bromine in concentrated hydrochloric acid.

METHOD FOR PRODUCING AMINOTHIAZOLE DERIVATIVE AND PRODUCTION INTERMEDIATE

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, (2008/06/13)

Provided is a method for selectively demethylating a 2-methoxy group. Specifically provided is a production method of a compound represented by formula (7) below through the following reactions.

METHOD FOR PRODUCING AMINOTHIAZOLE DERIVATIVE AND PRODUCTION INTERMEDIATE

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Page/Page column 11, (2010/10/20)

Disclosed is a selective demethylation process of a 2-methoxy group. Specifically disclosed is a method for producing a compound represented by the formula (7) below through the following reactions.

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