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6512-25-0

Dimethyl 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)benzene-1,3-dicarboxylate is a complex organic compound with the molecular formula C13H14O8. It is a derivative of benzene, featuring two hydroxyl groups at the 2 and 4 positions, and a methoxy-oxoethyl group at the 6 position. The compound also has two ester groups attached to the 1 and 3 positions of the benzene ring, which are derived from carboxylic acid groups. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and other chemical products due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions involving benzene derivatives and is used as an intermediate in the production of certain drugs and other specialty chemicals.

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  • 6512-25-0 Structure

  • Basic information

    1. Product Name: dimethyl 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)benzene-1,3-dicarboxylate
    2. Synonyms: 1,3-benzenedicarboxylic acid, 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)-, dimethyl ester; 2,4-Dihydroxy-6-methoxycarbonylmethyl-isophthalic acid dimethyl ester; Dimethyl 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)isophthalate; Phenylacetic acid, 2,4-dimethoxycarbonyl-3,5-dihydroxy-, methyl ester
    3. CAS NO:6512-25-0
    4. Molecular Formula: C13H14O8
    5. Molecular Weight: 298.2455
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6512-25-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 421.6°C at 760 mmHg
    3. Flash Point: 155.4°C
    4. Appearance: N/A
    5. Density: 1.387g/cm3
    6. Vapor Pressure: 1.05E-07mmHg at 25°C
    7. Refractive Index: 1.56
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: dimethyl 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)benzene-1,3-dicarboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: dimethyl 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)benzene-1,3-dicarboxylate(6512-25-0)
    12. EPA Substance Registry System: dimethyl 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)benzene-1,3-dicarboxylate(6512-25-0)

  • 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: 6512-25-0(Hazardous Substances Data)

6512-25-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6512-25-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,1 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6512-25:
(6*6)+(5*5)+(4*1)+(3*2)+(2*2)+(1*5)=80
80 % 10 = 0
So 6512-25-0 is a valid CAS Registry Number.

6512-25-0SDS

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 dimethyl 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)benzene-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 2,4-Dihydroxy-6-methoxycarbonylmethyl-isophthalic acid dimethyl 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:6512-25-0 SDS

6512-25-0Relevant articles and documents

Xylochemical synthesis and biological evaluation of shancigusin c and bletistrin g

Efferth, Thomas,Geske, Leander,Kauhl, Ulrich,Opatz, Till,Saeed, Mohamed E. M.,Schüffler, Anja,Thines, Eckhard

supporting information, (2021/06/16)

The biological activities of shancigusin C (1) and bletistrin G (2), natural products isolated from orchids, are reported along with their first total syntheses. The total synthesis of shancigusin C (1) was conducted by employing the Perkin reaction to forge the central stilbene core, whereas the synthesis of bletistrin G (2) was achieved by the Wittig olefination followed by several regiose-lective aromatic substitution reactions. Both syntheses were completed by applying only renewable starting materials according to the principles of xylochemistry. The cytotoxic properties of shancigusin C (1) and bletistrin G (2) against tumor cells suggest suitability as a starting point for further structural variation.

Synthesis of functionally substituted furan and resorcinol derivatives from dimethyl 3-oxopentanedioate

Ismailov,Ibragimova,Sadykhova,Mamedova,Yusubov

, p. 950 - 952 (2017/08/02)

The alkylation of dimethyl 3-oxopentanedioate with 1,2-dibromoethane and 1,2,3-tribromopropane afforded C,C-(cyclopropane derivative) and C,O-dialkylation products. The initial trioxo compound underwent partial self-condensation to produce resorcinol deri

Syntheses of Naturally Occuring 5-Carbonylmethyl-7-hydroxy-2-methyl-chromones and -chromanone (Studies on the β-Carbonyl Compounds Connected with the β-Polyketides. X)

Takeuchi, Naoki,Sasaki, Yuki,Kosugi, Yoko,Tobinaga, Seisho

, p. 2012 - 2015 (2007/10/02)

Naturally occuring 5-carbonylmethyl-7-hydroxy-2-methyl-chromones, -chromanone and an analogue 1, 2, 3, and 4 were synthesized by two routes from a self condensation product 6 of dimethyl acetonedicarboxylate, and the pyrone 10.

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