CAS 50-62-4
:Benzoic acid, 3,4,5-trimethoxy-, 1,2-ethanediylbis[(methylimino)-3,1-propanediyl] ester, dihydrochloride
Description:
The chemical substance known as "Benzoic acid, 3,4,5-trimethoxy-, 1,2-ethanediylbis[(methylimino)-3,1-propanediyl] ester, dihydrochloride" with CAS number 50-62-4 is a complex organic compound characterized by its structure, which includes a benzoic acid moiety substituted with three methoxy groups at the 3, 4, and 5 positions. This compound features a diester linkage involving a 1,2-ethanediyl group and methylimino groups, contributing to its unique chemical properties. As a dihydrochloride salt, it is likely to be soluble in water, which is a common characteristic of many hydrochloride salts. The presence of multiple functional groups suggests potential reactivity, particularly in biological systems, where it may exhibit pharmacological activity. Its molecular structure indicates that it could participate in hydrogen bonding and other intermolecular interactions, influencing its solubility and stability. Overall, this compound's intricate structure and functional groups make it of interest in various fields, including medicinal chemistry and organic synthesis.
Formula:C30H44N2O10·2ClH
InChI:InChI=1/C30H44N2O10.ClH/c1-31(11-9-15-41-29(33)21-17-23(35-3)27(39-7)24(18-21)36-4)13-14-32(2)12-10-16-42-30(34)22-19-25(37-5)28(40-8)26(20-22)38-6;/h17-20H,9-16H2,1-8H3;1H
InChI key:InChIKey=GIOKUMNZQFCEPI-UHFFFAOYSA-N
SMILES:O(C)C1=C(OC)C=C(C(OCCCN(CCN(CCCOC(=O)C2=CC(OC)=C(OC)C(OC)=C2)C)C)=O)C=C1OC.Cl
Synonyms:- 1-Propanol, 3,3′-[ethylenebis(methylimino)]di-, bis(3,4,5-trimethoxybenzoate) (ester), dihydrochloride
- Andiamine
- Benzoic acid, 3,4,5-trimethoxy-, 1,2-ethanediylbis((methylimino)-3,1-propanediyl) ester, 2HCl
- Benzoic acid, 3,4,5-trimethoxy-, 1,2-ethanediylbis[(methylimino)-3,1-propanediyl] ester, dihydrochloride
- Benzoic acid, 3,4,5-trimethoxy-, diester with 3,3'-(ethylenebis(methylimino))di-1-propanol, dihydrochloride
- Ethane-1,2-Diylbis[(Methylimino)Propane-3,1-Diyl] Bis(3,4,5-Trimethoxybenzoate) Dihydrochloride
- Ethane-1,2-Diylbis[(Methylimino)Propane-3,1-Diyl] Bis(3,4,5-Trimethoxybenzoate) Hydrochloride
- Flussicor
- Hexobendin hydrochloride
- Hexobendine HCl
- N,N'-Dimethyl-N,N'-bis(3-(3',4',5'-trimethoxybenzoxy)propyl)ethylenediamine dihydrochloride
- Reoxyl
- Ustimon
- Hexobendine dihydrochloride
- 3,3'-[Ethylenebis(MethyliMino)]di-1-propanol Bis(3,4,5-triMethoxybenzoate) (Ester) Dihydrochloride
- 3,4,5-trimethoxybenzoic acid 3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxybenzoyl)oxypropyl]amino]ethyl]amino]propyl ester dihydrochloride
- 3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxyphenyl)carbonyloxypropyl]amino]ethyl]amino]propyl 3,4,5-trimethoxybenzoate dihydrochloride
- 3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxybenzoyl)oxypropyl]amino]ethyl]amino]propyl 3,4,5-trimethoxybenzoate dihydrochloride
- HEXOBENDINEHYDROCHLORIDE
- 3,4,5-TriMethoxybenzoic Acid 1,2-Ethanediylbis[(MethyliMino)-3,1-propanediyl] Ester Dihydrochloride
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Found 2 products.
Hexobendine dihydrochloride
CAS:<p>Hexobendine is a drug used to treat bowel disease and infectious diseases. It has been shown to stimulate the uptake of adenosine, which is an important mediator in energy metabolism. Hexobendine also increases the activity of enzymes involved in protein synthesis and other physiological effects. It inhibits the rate constant for a reaction by binding to an enzyme that does not bind to hexobendine, thereby changing the conformation of the enzyme active site and altering the reaction mechanism. Hexobendine's mode of action is similar to that of x-ray contrast media, which are used during diagnostic procedures such as x-rays or MRIs. The only difference is that x-ray contrast media are not absorbed by tissues, but instead create shadows on x-rays or MRIs.</p>Formula:C30H44N2O10•(HCl)2Purity:Min. 95%Color and Shape:PowderMolecular weight:665.6 g/molHexobendine Dihydrochloride
CAS:Controlled Product<p>Applications Hexobendine is used as vasodilator (coronary).<br>References Rdudolph, et al.: Arzneim.-Forsch., 20, 637 (1970), Kolassa, P., et al.: Biochem. Pharmacol., 20, 490 (1971), Zommer-Urbanska, S., et al.: Pharmazie, 40, 419 (1985),<br></p>Formula:C30H44N2O10·2ClHColor and Shape:NeatMolecular weight:665.60

