Sigma-Aldrich 147532 1,3,5-Benzenetricarbonyl trichloride 98% 10 gr
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Marka
Stok Kodu
LB.SA.147532-10G
Kısa Bilgi
Synonym(s): Benzene-1,3,5-tricarbonyl chloride, Trimesic acid trichloride, Trimesoyl chloride Linear Formula: C6H3(COCl)3 CAS Number: 4422-95-1 Molecular Weight: 265.48 Beilstein: 2940936 EC Number: 224-594-8 MDL number: MFCD00000679 PubChem Substance ID: 24848560 NACRES: NA.23
Bilgi
CAS Number: 4422-95-1
| Sigma-Aldrich 147532 1,3,5-Benzenetricarbonyl trichloride 98% |
| Synonym(s): Benzene-1,3,5-tricarbonyl chloride, Trimesic acid trichloride, Trimesoyl chloride Linear Formula: C6H3(COCl)3 CAS Number: 4422-95-1 Molecular Weight: 265.48 Beilstein: 2940936 EC Number: 224-594-8 MDL number: MFCD00000679 PubChem Substance ID: 24848560 NACRES: NA.23 |
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PROPERTIES
Quality Level 200
Assay 98% form solid bp 180 °C/16 mmHg (lit.) mp 32-38 °C (lit.) solubility chloroform: soluble 10%, clear to very slightly hazy, colorless to faintly yellow density 1.487 g/mL at 25 °C (lit.) SMILES string ClC(=O)c1cc(cc(c1)C(Cl)=O)C(Cl)=O InChI 1S/C9H3Cl3O3/c10-7(13)4-1-5(8(11)14)3-6(2-4)9(12)15/h1-3H InChI key UWCPYKQBIPYOLX-UHFFFAOYSA-N DESCRIPTION General description 1,3,5-Benzenetricarbonyl trichloride reacts with propargyl alcohol to yield triprop-2-ynyl benzene-1,3,5-tricarboxylate[1]. Application 1,3,5-Benzenetricarbonyl trichloride was used in the synthesis of chiral azoaromatic dendrimeric systems[2]. It was used to study the structure of activated composite membranes containing organophosphorus extractants as carriers[3]. It was the starting material for two tritopic amides derived from 3- and 4-methylaminopyridine which self-assembled into nanoballs on treatment with palladium(II) nitrate in DMSO.[4] |
