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1,4-Benzenedicarboxylic acid, 2,5-diamino-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24260-55-7

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24260-55-7 Usage

Molecular structure

A benzene ring with a carboxylic acid group (-COOH) at the 1st and 4th positions, and an amino group (-NH2) at the 2nd and 5th positions, with a methyl ester group (-OCH3) attached to each carboxylic acid group.

Physical state

Clear, colorless liquid

Odor

Slightly sweet

Solubility

Highly soluble in organic solvents

Applications

a. Production of polyester resins and fibers
b. Manufacturing of polyethylene terephthalate (PET) and other polyester-based products
c. Precursor in the synthesis of various polymers
d. Used in pharmaceutical and agricultural industries

Safety precautions

a. Skin and eye irritant
b. Potential long-term health effects if not used properly
c. Handle with caution and follow safety guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 24260-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,6 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24260-55:
(7*2)+(6*4)+(5*2)+(4*6)+(3*0)+(2*5)+(1*5)=87
87 % 10 = 7
So 24260-55-7 is a valid CAS Registry Number.

24260-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2,5-diaminobenzene-1,4-dicarboxylate

1.2 Other means of identification

Product number -
Other names 2,5-diamino-terephthalic 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:24260-55-7 SDS

24260-55-7Downstream Products

24260-55-7Relevant academic research and scientific papers

Development of NIR emissive fully-fused bisboron complexes with π-conjugated systems including multiple azo groups

Chujo, Yoshiki,Gon, Masayuki,Nakamura, Masashi,Natsuda, Shin-Ichiro,Ohkita, Hideo,Tamai, Yasunari,Tanaka, Kazuo

supporting information, p. 74 - 84 (2021/12/27)

Development of novel near-infrared (NIR) emitters is essential for satisfying the growing demands of advancing optical telecommunication and medical technology. We synthesized elemental skeletons composed of robust π-conjugated systems including two boron-fused azo groups, which showed an intense emission in the red or near-infrared (NIR) region both in solution and solid states. Two types of bisboron complexes with different aromatic linkers showed emission properties with larger bathochromic shifts and emission efficiencies in solution than the corresponding monoboron complex. Transient absorption spectroscopy disclosed that the inferior optical properties of the monoboron complex can be attributed to fast nonradiative deactivation accompanied by a large structural relaxation after photoexcitation. The expanded π-conjugated system through multiple boron-fused azo groups can contribute to rigid molecular skeletons followed by improved emission properties. Moreover, theanti-form of the bisboron complex with fluorine groups in the opposite directions to the π-plane exhibited crystallization-induced emission enhancement in the NIR region. The molecular design by using multiple boron-fused azo groups is expected to be a critical strategy for creating novel NIR emitters.

3-SUBSTITUTED 1,2,3-TRIAZIN-4-ONE'S AND 3-SUBSTITUTED 1,3-PYRIMIDINONE'S FOR ENHANCING GLUTAMATERGIC SYNAPTIC RESPONSES

-

Page/Page column 103-104, (2009/04/25)

This invention relates to compounds, pharmaceutical compositions and methods for use in the prevention and treatment of cerebral insufficiency, including enhancement of receptor functioning in synapses in brain networks responsible for basic and higher order behaviors. These brain networks, which are involved in regulation of breathing, and cognitive abilities related to memory impairment, such as is observed in a variety of dementias, in imbalances in neuronal activity between different brain regions, as is suggested in disorders such as Parkinson''s disease, schizophrenia, respiratory depression, sleep apneas, attention deficit hyperactivity disorder and affective or mood disorders, and in disorders wherein a deficiency in neurotrophic factors is implicated, as well as in disorders of respiration such as overdose of an alcohol, an opiate, an opioid, a barbiturate, an anesthetic, or a nerve toxin, or where the respiratory depression results form a medical condition such as central sleep apnea, stroke- induced central sleep apnea, obstructive sleep apnea, congenital hypoventilation syndrome, obesity hypoventilation syndrome, sudden infant death syndrome, Rett syndrome, spinal cord injury, traumatic brain injury, Cheney-Stokes respiration, Ondines curse, Prader-Willi''s syndrome and drowning. In a particular aspect, the invention relates to compounds useful for treatment of such conditions, and methods of using these compounds for such treatment.

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