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4-(N-phenylacetylamino)-1,3,4,5-tetrahydrobenz[cd]indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147108-60-9

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147108-60-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147108-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,1,0 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 147108-60:
(8*1)+(7*4)+(6*7)+(5*1)+(4*0)+(3*8)+(2*6)+(1*0)=119
119 % 10 = 9
So 147108-60-9 is a valid CAS Registry Number.

147108-60-9Downstream Products

147108-60-9Relevant academic research and scientific papers

Syntheses of 4-amino-, 4-hydroxy-, and 4-nitro-1,3,4,5-tetrahydrobenz[cd]indoles and its bromination

Nakagawa, Kyoko,Aoki, Naokatsu,Mukaiyama, Harunobu,Somei, Masanori

, p. 493 - 520 (2014)

Simple synthetic method for 4-nitro-1,3,4,5-tetrahydrobenz[cd]indole (6) is established from indole-3-carboxaldehyde (7). With 6 in hand, various derivatives of 4-amino-, 4-hydroxy- and 4-amino-4-hydroxymethyl-1,3,4,5-tetrahydrobenz[cd]indoles become readily available. Bromination of 6 afforded useful building blocks for further manipulation. Successful optical resolution of 6 by chiral column chromatography is also reported.

A SIMPLE FOUR STEP SYNTHESIS AND OPTICAL RESOLUTION OF 4-NITRO-1,3,4,5-TETRAHYDROBENZINDOLE, AND THE SYNTHESES OF 1-HYDROXY DERIVATIVES OF 4-NITRO- AND 4-AMINO-1,3,4,5-TETRAHYDROBENZINDOLES

Nakagawa, Kyoko,Aoki, Naokatsu,Mukaiyama, Harunobu,Somei, Masanori

, p. 2269 - 2275 (2007/10/02)

4-Nitro-1,3,4,5-tetrahydrobenzindole was synthesized from indole-3-carboxaldehyde in four steps with an overall yield of 30percent.Optical resolution of its enantiomers by chiral column chromatography was successful.Syntheses of 1-hydroxy derivatives of 4-nitro- and 4-amino-1,3,4,5-tetrahydrobenzindoles are also reported.

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