1,2,3,4-Tetrahydrocyclopent[b]indole
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![1,2,3,4-Tetrahydrocyclopent[b]indole structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220812/3e190017653445278a2d23477a02e245.png "1,2,3,4-Tetrahydrocyclopent[b]indole")
1,2,3,4-Tetrahydrocyclopent[b]indole
structure -
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CAS No:
2047-91-8
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Formula:
C11H11N
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Chemical Name:
1,2,3,4-Tetrahydrocyclopent[b]indole
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Synonyms:
Cyclopent[b]indole,1,2,3,4-tetrahydro-;1,2,3,4-Tetrahydrocyclopent[b]indole;2,3-Trimethyleneindole;1H-Indole,2,3-(1,3-propanediyl)-;NSC 112674;1,2,3,4-Tetrahydrocyclopenta[b]indole;1H,2H,3H,4H-Cyclopenta[b]indole
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CAS No:
1,2,3,4-Tetrahydrocyclopent[b]indole Basic Attributes
157.21
157.21
112674
DTXSID10296917
2933990090
Safety Information
NONH for all modes of transport
3
R36/37/38
26-36
Xi: Irritant;
P261-P305 + P351 + P338
H315-H319-H335
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 39 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
1,2,3,4-Tetrahydrocyclopent[b]indole Use and Manufacturing
• ;Reactant for thionium species-mediated functionalization at the 2α-position of indoles1• ;Reactant for preparation of tetramethylpiperidine-1-oxoammonium salts as oxidants2
Computed Properties
Molecular Weight:157.21
XLogP3:2.7
Hydrogen Bond Donor Count:1
Exact Mass:157.089149355
Monoisotopic Mass:157.089149355
Topological Polar Surface Area:15.8
Heavy Atom Count:12
Complexity:178
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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1,2,3,4-Tetrahydrocyclopent[b]indole
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