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5870-37-1

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5870-37-1 Usage

General Description

1,4-Benzenedicarboxylic acid, 2,5-dihydroxy-, dimethyl ester, also known as dimethyl 2,5-dihydroxyterephthalate, is an organic compound primarily used in the field of organic synthesis. This colorless, crystalline substance is a derivative of terephthalic acid and includes two ester functional groups, two carboxyl groups, and two hydroxyl groups. It possesses unique physical and chemical properties including a molecular weight of 226.22 g/mol and exhibits good stability under normal temperature and pressure. Due to its specific structure, it is often utilized in applications like various types of polymerization reactions and as an intermediate in the production of polyester resins, plasticizers, and other polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 5870-37-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5870-37:
(6*5)+(5*8)+(4*7)+(3*0)+(2*3)+(1*7)=111
111 % 10 = 1
So 5870-37-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O6/c1-15-9(13)5-3-8(12)6(4-7(5)11)10(14)16-2/h3-4,11-12H,1-2H3

5870-37-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-Dihydroxybenzol-1,4-dicarbonsaeure-dimethylester

1.2 Other means of identification

Product number -
Other names dimethyl 2,5-dihydroxy-1,4-benzenedicarboxylate

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:5870-37-1 SDS

5870-37-1Relevant articles and documents

Supramolecular 2D monolayered nanosheets constructed by using synergy of non-covalent interactions

Ding, Qinwen,Dong, Zeyuan,Qi, Shuaiwei,Wang, Wenzhe,Zhang, Chenyang,Zhang, Hongyu,Zhang, Jing

, p. 6272 - 6275 (2021)

Here, a straightforward and rational approach to construct supramolecular assemblies with ordered nanostructures in a two-dimensional arrangement is reported. Taking advantage of the synergistic effect of multiple non-covalent interactions (hydrogen bonding and π-π interactions), the designed molecular monomer has a specific orientation in the self-assembly process, thus realizing two-dimensional control. Supramolecular two-dimensional nanosheets with single-layer thickness and controllable dimensions have been obtained, which can be clearly confirmed using TEM, SEM, AFM and XRD and by comparing with the self-assembled structures of the control system. The strategy of collaborative self-assembly proposed here using multiple non-covalent interactions is expected to be extended to the construction of various kinds of unique supramolecular 2D materials. This journal is

Synthesis and antimicrobial activities of 2,5-substituent hydroquinone derivatives

Liu, Hui-Lian,Wang, Qing-Zhong

, p. 5165 - 5167 (2014)

A series of 2,5-substituent hydroquinone derivatives were designed and synthesized. Their structures were identified by elemental analysis, 1H NMR, IR spectra. Their assayed antibacterial (Escherichia coli, Bacillus subtilis) and antifungal (Candida albicans) activities were also evaluated by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) method. The results of biological test showed compounds 1 and 10 have favorable antimicrobial activity with MICs of 20.5, 24.6, 18.9 and 28.6 μg/mL against Escherichia coli and Bacillus subtilis, respectively.

Amidation, Esterification, and Thioesterification of a Carboxyl-Functionalized Covalent Organic Framework

Guo, Lei,Jia, Shang,Diercks, Christian S.,Yang, Xuejing,Alshmimri, Sultan A.,Yaghi, Omar M.

, p. 2023 - 2027 (2020)

Three new post-synthetic modification reactions, namely amidation, esterification, and thioesterification, were demonstrated on a novel highly crystalline two-dimensional covalent organic framework (COF), COF-616, bearing pre-installed carboxyl groups. Th

EUROPIUM BASED METAL ORGANIC FRAMEWORK FOR PALLADIUM SENSING

-

Paragraph 0090, (2021/01/26)

A method of detecting Pd2+ in an aqueous solution is described. The method involves mixing an Eu-based metal organic framework with the aqueous solution and measuring the amount of fluorescence quenching. The fluorescence quenching is specific

Fine-tuning the pore structure of metal-organic frameworks by linker substitution for enhanced hydrogen storage and gas separation

Han, Xiwei,Yang, Xiaoxian,Yu, Chuan,Lu, Shuyan,Pouya, Ehsan Sadeghi,Bai, Peng,Lyu, Jiafei,Guo, Xianghai

, p. 3026 - 3032 (2021/05/03)

The modification of metal-organic frameworks (MOFs) by functionalizing ligands has been investigated for improved properties. In this study, by introducing substituents to the backbone of organic linkers, isostructural dihydroxy-/dialkoxy-functionalized Zr-MOFs were delicately constructed and sophisticatedly characterized for crystallinity, morphology, porosity and structural defects. Pure-component CO2, CH4, N2, and H2adsorption isotherms on the microporous synthesized materials were investigated under the pressure up to 10 MPa at 303 K. By the ideal adsorbed solution theory (IAST) model, enhanced adsorption selectivity towards CO2/N2, CO2/CH4, CH4/N2and CO2/H2binary mixtures was observed compared to the parent material, and dihydroxy functionalization endows the material with high selectivity towards CO2/H2. Moreover, the diethoxy-functionalized material with narrow cavities exhibits improved high pressure H2adsorption due to structural defects and strong overlapping potentials.

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