96933-21-0

Basic information

• Product Name: A-3,4,5-TETRAHYDROBENZ(CD)INDOL-(1H)-ONE)
• Synonyms: A-3,4,5-TETRAHYDROBENZ(CD)INDOL-(1H)-ONE);2a,3,4,5-Tetrahydro-1-azaacenaphthylen-2(1H)-one;2(1H)-ONE, 2A,3,4,5-TETRAHYDRO-BENZ[CD]INDOL
• CAS NO: 96933-21-0
• Molecular Formula: C₁₁H₁₁NO
• Molecular Weight: 173.21
• Mol File: 96933-21-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: A-3,4,5-TETRAHYDROBENZ(CD)INDOL-(1H)-ONE)(CAS DataBase Reference)
• NIST Chemistry Reference: A-3,4,5-TETRAHYDROBENZ(CD)INDOL-(1H)-ONE)(96933-21-0)
• EPA Substance Registry System: A-3,4,5-TETRAHYDROBENZ(CD)INDOL-(1H)-ONE)(96933-21-0)

Safety Data

• Hazardous Substances Data: 96933-21-0(Hazardous Substances Data)

Upstream product

• 138206-98-1 (+/-)-1,2,2a,3,4,5-hexahydro-2-oxobenzindole-1,2a-dicarbaldehyde tetraethyl acetal 
• 130-00-7 1,8-naphtholactam 
• 138343-71-2 1-(tert-butoxycarbonyl)-5,6,7,8-tetrahydronaphthylamine 
• 2217-41-6 1-amino-5,6,7,8-tetrahydronaphthalene 
• 138343-74-5 8-tert-Butoxycarbonylamino-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid methyl ester 

Downstream Products

• 177963-27-8 4,5-Dihydro-1H-benzo[cd]indol-2-one 
• 125030-68-4 2a-{3-[4-(2-Chloro-phenyl)-9-methyl-6H-1-thia-5,7,8,9a-tetraaza-cyclopenta[e]azulen-2-yl]-prop-2-ynyl}-2a,3,4,5-tetrahydro-1H-benzo[cd]indol-2-one 
• 125030-74-2 1-{3-[4-(2-Chloro-phenyl)-9-methyl-6H-1-thia-5,7,8,9a-tetraaza-cyclopenta[e]azulen-2-yl]-prop-2-ynyl}-2a-methyl-2a,3,4,5-tetrahydro-1H-benzo[cd]indol-2-one 
• 201608-92-6 C₂₇H₃₁N₃O*ClH 
• 201608-58-4 C₂₇H₃₅N₃O*ClH 
• 201608-52-8 C₂₆H₃₃N₃O₂*ClH 
• 201608-50-6 C₂₆H₃₃N₃O*ClH 
• 201608-56-2 C₂₅H₃₀ClN₃O*ClH 
• 201608-38-0 C₂₆H₃₃N₃O₂*ClH 
• 201608-48-2 C₂₆H₃₃N₃O₂*ClH 
• 201608-96-0 C₂₇H₃₄N₂O*ClH 
• 201608-66-4 C₂₇H₃₂N₂O*ClH 
• 201608-60-8 C₂₅H₃₁N₃O₂*ClH 
• 201608-75-5 C₂₆H₃₃N₃O*ClH 

Relevant articles and documents

Diethoxymethyl: A useful nitrogen-protecting group for lactams and amides

Treatment of the lactams 3a-e and the amide 3f with triethyl orthoformate leads to the N-diethoxymethyl substituted derivatives 4a-f. Additionally, the indolinones 3a and 3b can react at the lactam α-position to give the reaction products 2 and 5, respectively. The diethoxymethyl group can be easily removed by subsequent treatment with trifluoroacetic acid and NaOH.

Cyclic amidines derived from benz[c,d]indole and 4,5-dihydro-3H-1-benzazepine including some related compounds: Synthesis and pharmacological screening

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