13438-29-4

Basic information

• Product Name: 1,3-Benzenedicarbonyl dichloride, 5-methyl-
• Synonyms: 5-methylisophthaloyl dichloride;5-Methyl-isophthaloylchlorid;5-methylisophthaloyl chloride;1,3-Benzenedicarbonyl dichloride,5-methyl
• CAS NO: 13438-29-4
• Molecular Formula: C9H6Cl2O2
• Molecular Weight: 217.051
• Mol File: 13438-29-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1,3-Benzenedicarbonyl dichloride, 5-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Benzenedicarbonyl dichloride, 5-methyl-(13438-29-4)
• EPA Substance Registry System: 1,3-Benzenedicarbonyl dichloride, 5-methyl-(13438-29-4)

Safety Data

• Hazardous Substances Data: 13438-29-4(Hazardous Substances Data)

Upstream product

• 499-49-0 5-methylisophthalic aicd 

Downstream Products

• 1080498-57-2 C₂₁H₂₈O₄ 
• 17649-58-0 5-Methylisophthalsaeure-dimethylester 
• 42268-88-2 1,3-dimethyl 5-(bromomethyl)benzene-1,3-dicarboxylate 
• 422550-81-0 N,N'-dimethoxy-N,N',5-trimethylisophthalamide 
• 39718-07-5 5-methylbenzene-1,3-dicarbonitrile 
• 87533-36-6 C₁₃H₂₀N₈*2ClH 
• 87533-52-6 1,3-diacetyl-5-methylbenzene 
• 90868-23-8 5-methyl-isophthalic acid diamide 

Relevant articles and documents

COMPOUND, POLYMER, PATTERN FORMING MATERIAL, AND MANUFACTURING METHOD OF SEMICONDUCTOR DEVICE

A pattern forming material is configured to use for forming an organic film on a film to be processed, patterning the organic film, and then forming a composite film by infiltrating a metallic compound into the patterned organic film. The pattern forming material contains a polymer including a monomer unit represented by a general formula (3) described below, where R21 is H or CH3, each R22 is a hydrocarbon group of C2-14 where α carbon is primary carbon, secondary carbon or tertiary carbon, Q is a single bond or a hydrocarbon group of C1-20 carbon atoms which may include an oxygen atom, a nitrogen atom, or a sulfur atom between carbon-carbon atoms of or at a bond terminal, and a halogen atom may be substituted for the hydrogen atom.

Identification and SAR Evaluation of Hemozoin-Inhibiting Benzamides Active against Plasmodium falciparum

Quinoline antimalarials target hemozoin formation causing a cytotoxic accumulation of ferriprotoporphyrin IX (Fe(III)PPIX). Well-developed SAR models exist for β-hematin inhibition, parasite activity, and cellular mechanisms for this compound class, but no comparably detailed investigations exist for other hemozoin inhibiting chemotypes. Here, benzamide analogues based on previous HTS hits have been purchased or synthesized. Only derivatives containing an electron deficient aromatic ring and capable of adopting flat conformations, optimal for π-π interactions with Fe(III)PPIX, inhibited β-hematin formation. The two most potent analogues showed nanomolar parasite activity, with little CQ cross-resistance, low cytotoxicity, and high in vitro microsomal stability. Selected analogues inhibited hemozoin formation in Plasmodium falciparum causing high levels of free heme. In contrast to quinolines, introduction of amine side chains did not lead to benzamide accumulation in the parasite. These data reveal complex relationships between heme binding, free heme levels, cellular accumulation, and in vitro activity of potential novel antimalarials.

5-Substituted isophthalate-based organic electrochromic materials

A new series of isophthalate-based electrochromic materials were prepared. The functional groups at the 5-position of isophthalate have a significant influence on the observed color. In particular, an electrochemically active nitro group induced a multi-color display, indicating that further electrochromic properties could be manipulated using more diverse 5-substituted isophthalate derivatives. The Royal Society of Chemistry 2008.