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Diethyl (acetylamino)[(7-nitro-1H-indol-3-yl)methyl]propanedioate is a complex organic compound with the molecular formula C20H22N2O8. It is characterized by the presence of a 7-nitro-1H-indol-3-yl group, which is a substituted indole ring system, and an acetylamino group, indicating the presence of an amide derived from acetic acid. The compound also features a propanedioate (succinate) moiety, which is a dicarboxylic acid segment. This chemical structure suggests that it may have potential applications in pharmaceuticals or as a chemical intermediate due to its diverse functional groups and the presence of a nitro group, which can be involved in various chemical reactions. The compound's specific properties, such as solubility, stability, and reactivity, would depend on the context in which it is used and the conditions under which it is synthesized or stored.

1654-32-6

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1654-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1654-32-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1654-32:
(6*1)+(5*6)+(4*5)+(3*4)+(2*3)+(1*2)=76
76 % 10 = 6
So 1654-32-6 is a valid CAS Registry Number.

1654-32-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-acetamido-2-[(7-nitro-1H-indol-3-yl)methyl]propanedioate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:1654-32-6 SDS

1654-32-6Downstream Products

1654-32-6Relevant academic research and scientific papers

Synthesis and NMR characteristics of N-acetyl-4-nitro, N-acetyl-5-nitro, N-acetyl-6-nitro and N-acetyl-7-nitrotryptophan methyl esters

King, Russell R.,Calhoun, Larry A.

, p. 273 - 276 (2009)

N-acetyl-4-nitrotryptophan methyl ester (2), N-acetyl-5-nitrotryptophan methyl ester (3), N-acetyl-6-nitrotryptophan methyl ester (4) and N-acetyl-7-nitrotryptophan methyl ester (5) were synthesized through a modified malonic ester reaction of the appropriate nitrogramine analogs followed by methylation with BF3-methanol. Assignments of the 1H and 13C NMR chemical shifts were made using a combination of 1H-1H COSY, 1H-13C HETCOR and 1H-13C selective INEPT experiments. Copyright

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