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Catalog Number:
12108
CAS Number:
129848-93-7
L-1,2,3,4-Tetrahydronorharman-3-carboxylic acid ethyl ester hydrochloride
Purity:
≥ 95% (HPLC)
Synonym(s):
L-1,2,3,4-Tetrahydronorharman-3-carboxylic acid ethyl ester hydrochloride
Documents
$67.60 /250MG
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Product Information

L-1,2,3,4-Tetrahydronorharman-3-carboxylic acid ethyl ester hydrochloride is a versatile compound recognized for its significant applications in pharmaceutical research and development. This compound, a derivative of the norharman family, exhibits unique properties that make it valuable in the synthesis of various bioactive molecules. Its structure allows for potential interactions with biological systems, making it a candidate for studies related to neuropharmacology and the development of novel therapeutic agents. Researchers have utilized this compound in the exploration of neuroprotective effects and its role in modulating neurotransmitter systems, which could lead to advancements in treatments for neurological disorders.

In addition to its pharmaceutical relevance, L-1,2,3,4-Tetrahydronorharman-3-carboxylic acid ethyl ester hydrochloride serves as a useful intermediate in organic synthesis, particularly in the creation of complex heterocyclic compounds. Its ability to facilitate various chemical reactions enhances its appeal to chemists and researchers looking to innovate in drug design and development. The compound's stability and reactivity make it an excellent choice for those seeking to expand their research capabilities in medicinal chemistry.

Synonyms
L-1,2,3,4-Tetrahydronorharman-3-carboxylic acid ethyl ester hydrochloride
CAS Number
129848-93-7
Purity
≥ 95% (HPLC)
Molecular Formula
C14H16N2O2·HCl
Molecular Weight
280.74
MDL Number
MFCD22690656
PubChem ID
6602999
Conditions
Store at 0-8°C
General Information
Synonyms
L-1,2,3,4-Tetrahydronorharman-3-carboxylic acid ethyl ester hydrochloride
CAS Number
129848-93-7
Purity
≥ 95% (HPLC)
Molecular Formula
C14H16N2O2·HCl
Molecular Weight
280.74
MDL Number
MFCD22690656
PubChem ID
6602999
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

L-1,2,3,4-Tetrahydronorharman-3-carboxylic acid ethyl ester hydrochloride is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Neuroscience Research: It is used in studies investigating the effects of psychoactive compounds on the brain, providing insights into mental health treatments and cognitive function.
  • Analytical Chemistry: The compound is employed as a standard in chromatographic techniques, aiding in the accurate quantification of related substances in complex mixtures.
  • Natural Product Synthesis: It plays a role in the synthesis of natural alkaloids, which are important for developing new therapeutic agents derived from plant sources.
  • Biochemical Assays: This chemical is utilized in various assays to evaluate biological activity, helping researchers understand its potential therapeutic effects and mechanisms of action.

Citations