cas 61894-99-3|| where to buy 2,3,4,9-tetrahydro-1H-carbazol-3-amine

製品名:2,3,4,9-tetrahydro-1H-carbazol-3-amine

IUPAC Name:2,3,4,9-tetrahydro-1H-carbazol-3-amine

: CAS番号：61894-99-3; 分子式：C12H14N2; 純度：97%

: カタログ番号：CM254071; 分子量：186.26

包装単位	有効在庫	価格（USD）	数量
CM254071-5g	in stock	ǸŤǙ

問い合わせ: sales@chemenu.com

研究開発用専用.

問い合わせフォーム

化学物質名

CAS番号

数量*

要求仕様*
（アッセイ %、材料グレード等）

お名前*

連絡先Eメールアドレス*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 61894-99-3 regularly via the above email.

追記事項

Verification code*

refresh

製品詳細

: CAS番号:61894-99-3; 分子式:C12H14N2; 融点:-; SMILESコード:NC1CCC(NC2=C3C=CC=C2)=C3C1; 密度:

: カタログ番号:CM254071; 分子量:186.26; 沸点:; MDL番号:MFCD02181027; 保管方法:Keep in dark place, store at 2-8°C.

Category Infos

: Carbazoles; Carbazoles are an important class of nitrogen-containing heterocycles with a planar tricyclic skeleton consisting of two benzene rings fused on both sides of the central pyrrole ring, with a large aromatic system and a central nitrogen atom, showing broad of electron delocalization. The structure of this compound is based on the indole structure, but in which a second benzene ring is fused to a five-membered ring at positions 2-3 of the indole. Carbazole structural motifs are widely found in, but not limited to, a large number of natural alkaloids of plant or bacterial origin. Since many of these alkaloids are medically useful, exhibit a fairly wide range of biological activities (anticancer, anti-HIV, antibacterial, anti-Alzheimer's disease, anticoagulant, analgesic, antiepileptic, antidiabetic, antioxidant, etc.). Medicinal chemistry also uses carbazole motifs in synthetic drugs to combat hypertension, heart disease, and hepatitis C virus replication.; carbazole price; Buy low price, high quality carbazole,choose our products, warmly welcome new and old customers to visit and patronize!

Column Infos

: Indoles; Indole is a compound of pyrrole and benzene in parallel, also known as benzopyrrole. There are two combinations of pyrrole and benzene, called indole and isoindole, respectively. Many derivatives of indole have physiological and pharmacological activities, and can synthesize vasodilators, antihistamines, antipyretic analgesics, etc. in medicine, so indole is also a very important heterocyclic compound.

Product Other Information

Product Overview	2,3,4,9-tetrahydro-1H-carbazol-3-amine (THCA) is a compound derived from the amino acid tryptophan. It is a naturally occurring component of many plants, including Cannabis sativa, and is the precursor to the psychoactive component of cannabis, tetrahydrocannabinol (THC). THCA is a non-psychoactive compound and has been studied for its potential therapeutic applications.
Synthesis and Application	2,3,4,9-tetrahydro-1H-carbazol-3-amine can be synthesized from tryptophan using a variety of methods. The most common method is the catalytic hydrogenation of tryptophan in the presence of a metal catalyst and a hydrogen source. This method produces a mixture of 2,3,4,9-tetrahydro-1H-carbazol-3-amine and other compounds, which can then be separated and purified. Other methods of synthesis include the oxidative cleavage of tryptophan with a reagent such as nitric acid or peracetic acid, and the hydrolysis of tryptophan in the presence of a base. 2,3,4,9-tetrahydro-1H-carbazol-3-amine has been studied for its potential therapeutic applications, including anti-inflammatory and anti-cancer properties. It has been shown to inhibit the growth of certain cancer cell lines, and to reduce inflammation in animal models. In addition, 2,3,4,9-tetrahydro-1H-carbazol-3-amine has been studied for its potential role in the treatment of neurological disorders such as Alzheimer’s, Parkinson’s, and Huntington’s diseases.
Future Directions	The potential therapeutic applications of 2,3,4,9-tetrahydro-1H-carbazol-3-amine are still being explored. Further research is needed to better understand its mechanism of action, and to determine its efficacy in treating various diseases. In addition, further research is needed to develop methods for separating and purifying 2,3,4,9-tetrahydro-1H-carbazol-3-amine from other compounds in a laboratory setting, and to develop methods for measuring its effects in animal models. Finally, further research is needed to explore the potential for using 2,3,4,9-tetrahydro-1H-carbazol-3-amine in combination with other compounds for the treatment of various diseases.