(3-Chloropropyl)(3,4-dimethoxyphenethyl)methylammonium hydrogen oxalate

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1.What is the (3-Chloropropyl)(3,4-dimethoxyphenethyl)methylammonium hydrogen oxalate ?

(3-Chloropropyl)(3,4-dimethoxyphenethyl)methylammonium hydrogen oxalate is a quaternary ammonium compound characterized by a long alkyl chain with a chlorine atom at one end and a phenethyl group at the other end. It also features two methoxy groups attached to the phenethyl ring and is in the form of a hydrogen oxalate salt. (3-Chloropropyl)(3,4-dimethoxyphenethyl)methylammonium hydrogen oxalate may hold potential applications in organic synthesis and pharmaceutical research, although further investigation is required to determine its specific uses and properties.

2.What is the CAS number for (3-Chloropropyl)(3,4-dimethoxyphenethyl)methylammonium hydrogen oxalate ?

The CAS number of (3-Chloropropyl)(3,4-dimethoxyphenethyl)methylammonium hydrogen oxalate is 85226-25-1.

3.What are another words for (3-Chloropropyl)(3,4-dimethoxyphenethyl)methylammonium hydrogen oxalate ?

Synonyms?for?(3-Chloropropyl)(3,4-dimethoxyphenethyl)methylammonium hydrogen oxalate 85226-25-1:

4.What is (3-Chloropropyl)(3,4-dimethoxyphenethyl)methylammonium hydrogen oxalate (85226-25-1) used for?

Used in Organic Synthesis:
(3-Chloropropyl)(3,4-dimethoxyphenethyl)methylammonium hydrogen oxalate is used as a synthetic building block for [application reason] in the field of organic synthesis. Its unique structural features, including the quaternary ammonium group and the hydrogen oxalate salt form, may facilitate the creation of novel chemical entities with potential applications in various industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3-Chloropropyl)(3,4-dimethoxyphenethyl)methylammonium hydrogen oxalate is used as a starting material or intermediate for [application reason]. Its structural complexity and the presence of functional groups make it a promising candidate for the development of new drugs, particularly those targeting specific biological receptors or enzymes.

InChI:InChI=1/C14H22ClNO2.C2H2O4/c1-16(9-4-8-15)10-7-12-5-6-13(17-2)14(11-12)18-3;3-1(4)2(5)6/h5-6,11H,4,7-10H2,1-3H3;(H,3,4)(H,5,6)/p-1

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