| Company Name: |
Energy Chemical
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| Tel: |
021-58432009 400-005-6266 |
| Email: |
marketing@energy-chemical.com |
| Products Intro: |
Product Name:(R,R)-Chanoclavine
CAS:2390-99-0
Purity:NULL Package:10mg;1mg;2.5mg;5mg Remarks:NULL
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| Company Name: |
Cdreamlab (Hubei) Technology Co., LTD
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| Tel: |
0717-6300888 18062399888 |
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service@cdreamlab.com |
| Products Intro: |
Product Name:chanoclavine
CAS:2390-99-0
Purity:>=95% Package:100G;10KG;100KG
|
| Company Name: |
CLEARSYNTH LABS LTD.
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| Tel: |
+91-22-45045900 |
| Email: |
sales@clearsynth.com |
| Products Intro: |
Product Name:"(R,R)-Chanoclavine"
CAS:2390-99-0
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| | chanoclavine Basic information |
| Product Name: | chanoclavine | | Synonyms: | (E)-2-Methyl-3-[(1,3,4,5-tetrahydro-4β-(methylamino)benz[cd]indol)-5α-yl]-2-propen-1-ol;(E)-2-Methyl-3-[(4R,5R)-1,3,4,5-tetrahydro-4-(methylamino)benz[cd]indol-5-yl]-2-propen-1-ol;Secaclavine;2-Propen-1-ol, 2-methyl-3-[(4R,5R)-1,3,4,5-tetrahydro-4-(methylamino)benz[cd]indol-5-yl]-, (2E)- | | CAS: | 2390-99-0 | | MF: | C16H20N2O | | MW: | 256.34 | | EINECS: | | | Product Categories: | | | Mol File: | 2390-99-0.mol |  |
| | chanoclavine Chemical Properties |
| Melting point | 220-222° | | alpha | D20 -240° (pyridine); D20 -205° (c = 0.75 in alcohol) | | Boiling point | 470.1±45.0 °C(Predicted) | | density | 1.19±0.1 g/cm3(Predicted) | | pka | 14.74±0.10(Predicted) |
| | chanoclavine Usage And Synthesis |
| Uses | (R,R)-Chanoclavine is a modified ergot alkaloid produced by fungus. Stimulates dopamine receptors in the brain in rodents. | | Definition | ChEBI: Chanoclavine-I is an organic tricyclic compound that is 1,3,4,5-tetrahydrobenzo[cd]indole which is substituted at position 4 by a methylamino group and at position 5 by a 3-hydroxy-2-methylprop-1-en-1-yl group (the 4R,5R,E diastereoisomer). It is a precursor of the tetracyclic ergolines agroclavine, elymoclavine and lysergic acid amide. It is an ergot alkaloid, a benzoindole, a secondary amino compound, a primary alcohol and an organic heterotricyclic compound. It is a conjugate base of a chanoclavine-I(1+). |
| | chanoclavine Preparation Products And Raw materials |
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