2653-09-0

Upstream product

• 108-45-2 m-phenylenediamine 
• 79-04-9 chloroacetyl chloride 
• 4015-58-1 monochloroacetic acid anhydride 
• 541-69-5 m-phenylenediamine dihydrochloride 

Downstream Products

• 112818-61-8 N,N'-(1,3-phenylene)bis(2-(piperidin-1-yl)acetamide) 
• 2653-12-5 N,N'-bis-pyridinioacetyl-m-phenylenediamine; dichloride 
• 100468-82-4 1,3-bis-(2-triethylammonio-acetylamino)-benzene; dichloride 
• 1197453-07-8 C₉₀H₁₄₆N₄O₁₂Si₄ 
• 1454883-19-2 N,N'-bis(1-oxoethyl piperidine-2-carbamodithioate)-1,3-diaminobenzene 
• 1454883-20-5 N,N'-bis(1-oxoethyl morpholine-2-carbamodithioate)-1,3-diaminobenzene 
• 1454883-18-1 N,N'-bis(1-oxoethyl diethylamine-2-carbamodithioate)-1,3-diaminobenzene 
• 1339792-15-2 1,3-bis(amidomethyl-2,2′-dipicolylamine)benzene 
• 97772-03-7 1,3-bis-(2-trimethylammonio-acetylamino)-benzene; dichloride 
• 111293-83-5 N,N'-(1,3-phenylene)bis(2-(diethylamino)acetamide) 

Relevant academic research and scientific papers

Assembly of ion channel mimics from a modular construction set

Ion channel mimics were assembled from a modular construction set consisting of core units, derived from polycarboxylate 18-crown-6 ethers, wall units, derived from macrocyclic tetraesters, and polar head groups which provide overall amphiphilic character

Highly Efficient and Selective Visible-Light Driven CO2Reduction by Two Co-Based Catalysts in Aqueous Solution

Photocatalytic CO2 reduction has been considered as a promising approach to solve energy and environmental problems. Nevertheless, developing inexpensive photocatalysts with high efficiency and selectivity remains a big challenge. In this study, two Co-ba

Synthesis and characterization of symmetrical liquid crystalline compounds based on oxazole and thaizole rings

Twelve compounds containing a sulphur- or oxygen-based heterocyclic core, 1,3- oxazole or 1,3-thiazole ring with hydroxy, methoxy and methyl terminal substituent, were synthesized and characterized. The molecular structures of these compounds were perform

BIS(2-HALOACETAMIDO)-COMPOUNDS FOR USE AS LINKING AGENTS AND RESULTANT PRODUCTS WHICH COMPRISE ANTIBODIES, HALF-ANTIBODIES AND ANTIBODY FRAGMENTS

Bis(2-haloacetamido)- compounds for use as linkers to chemically cross-linking multiple thiol groups, and particularly, although not exclusively, the thiol groups of cysteine amino acids in peptide chains are described, along with their use as linking age

A simple and eco-compatible one-pot synthesis of new symmetrical dithiocarbamate podands and their dynamic NMR studies

A simple and eco-compatible synthesis of podands as 4a-i is performed using amines (3a-C), CS2, and dichlordiamides (DCDs) (2a, C) in the absence of a catalyst in water. Three reacting DCDs (2a-C) wer

Zinc selective chemosensor based on pyridyl-amide fluorescence

Chemosensors are developed to image zinc ions. Fluorescence enhancement due to Zn2+ binding is an excellent way to detect its presence. A chemosensor for Zn2+ based on dipicolylamine (DPA) groups connected by a pyridyl amide backbone

Membrane-length amphiphiles exhibiting structural simplicity and ion channel activity

A number of synthetic ion channels have been reported in recent years that incorporate unusual or sophisticated design elements. The present work demonstrates that extremely simple compounds can function as ion channels (insert in bilayers, exhibit open-c

Meta-bis anilide derivatives and their utility as herbicides

Compounds corresponding to the formula: SPC1 In which R1 and R2 are, independently, hydrogen, alkyl, alkoxyalkyl, cycloalkyl, pinonyl, ethylcycloalkyl, lower alkenyl, halogenated lower alkyl, benzyl, ethylphenyl, 2,4-dichlorophenoxy-methylene, styryl, furyl, phenyl or substituted phenyl in which the substituents are nitro, halogen, methyl, or methoxy; R3 and R4 are, independently, hydrogen or lower alkyl; X and Y are independently oxygen or sulfur; and Z is halogen, nitro, amino, lower alkyl, lower alkoxy or trifluoromethyl and n is an integer having a value from 0 to 4. The above compounds are effective herbicides, particularly for the control of grasses and broadleaf plants with both pre-emergence and post-emergence activity. Representative compounds are: m-propionamidobutyranilide, m-bis-2,2-dimethylvaleranilide, m-isobutyramido trichloroacetanilide, m-isobutyramido-2-ethylbutyranilide, m-t-butylacetamidopropionanilide, and 3'-N-ethyl propionamido-propionalide. This application is a continuation of application Ser. No. 180,916, filed Sept. 15, 1971, which is a continuation of application Ser. No. 20,104, filed Mar. 16, 1970, which is a continuation-in-part of application Ser. No. 741,267, filed July 1, 1968, which is a continuation-in-part of application Ser. No. 659,865, filed Aug. 11, 1967, all now abandoned.