Welcome to LookChem.com Sign In|Join Free

CAS

  • or

59092-92-1

2-(2,6-dihydroxy-4-methylbenzoyl)-5-hydroxy-3-methoxybenzoic acid is a complex organic compound with the molecular formula C16H14O8. It is a derivative of benzoic acid, featuring a benzene ring with various functional groups attached. The compound has two hydroxyl groups (-OH) at the 2nd and 6th positions, a methyl group (-CH3) at the 4th position, and a benzoyl group attached at the 2nd position. Additionally, it has a hydroxyl group at the 5th position and a methoxy group (-OCH3) at the 3rd position. This chemical structure endows the compound with unique properties and potential applications in various fields, such as pharmaceuticals, dyes, and materials science.

59092-92-1 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 59092-92-1 Structure

  • Basic information

    1. Product Name: 2-(2,6-dihydroxy-4-methylbenzoyl)-5-hydroxy-3-methoxybenzoic acid
    2. Synonyms:
    3. CAS NO:59092-92-1
    4. Molecular Formula: C16H14O7
    5. Molecular Weight: 318.2782
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 59092-92-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 652.749°C at 760 mmHg
    3. Flash Point: 245.776°C
    4. Appearance: N/A
    5. Density: 1.476g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.665
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(2,6-dihydroxy-4-methylbenzoyl)-5-hydroxy-3-methoxybenzoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(2,6-dihydroxy-4-methylbenzoyl)-5-hydroxy-3-methoxybenzoic acid(59092-92-1)
    12. EPA Substance Registry System: 2-(2,6-dihydroxy-4-methylbenzoyl)-5-hydroxy-3-methoxybenzoic acid(59092-92-1)

  • 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: 59092-92-1(Hazardous Substances Data)

59092-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59092-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,9 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59092-92:
(7*5)+(6*9)+(5*0)+(4*9)+(3*2)+(2*9)+(1*2)=151
151 % 10 = 1
So 59092-92-1 is a valid CAS Registry Number.

59092-92-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name demethylsulochrin

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:59092-92-1 SDS

59092-92-1Upstream product

59092-92-1Downstream Products

59092-92-1Relevant articles and documents

Bienzyme-Catalytic and Dioxygenation-Mediated Anthraquinone Ring Opening

Geng, Ce,Huang, Xuenian,Lu, Xuefeng,Qi, Feifei,Sun, Jia,Xue, Yingying,Zhang, Wei

supporting information, p. 16326 - 16331 (2021/10/20)

The C-10-C-4a bond cleavage of anthraquinone is believed to be a crucial step in fungal seco-anthraquinone biosynthesis and has long been proposed as a classic Baeyer-Villiger oxidation. Nonetheless, genetic, enzymatic, and chemical information on ring opening remains elusive. Here, a revised questin ring-opening mechanism was elucidated by in vivo gene disruption, in vitro enzymatic analysis, and 18O chasing experiments. It has been confirmed that the reductase GedF is responsible for the reduction of the keto group at C-10 in questin to a hydroxyl group with the aid of NADPH. The C-10-C-4a bond of the resultant questin hydroquinone is subsequently cleaved by the atypical cofactor-free dioxygenase GedK, giving rise to desmethylsulochrin. This proposed bienzyme-catalytic and dioxygenation-mediated anthraquinone ring-opening reaction shows universality.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 59092-92-1