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Benzamide, N-[2-methyl-1-[(propylamino)carbonyl]propyl]-3,5-dinitrois a synthetic chemical compound characterized by a complex molecular structure. It is composed of a benzamide core, a propylamino carbonyl group, and two nitro functional groups. Benzamide, N-[2-methyl-1-[(propylamino)carbonyl]propyl]-3,5-dinitrois potentially hazardous and may possess explosive or reactive properties, necessitating careful handling. Its structure suggests potential applications in chemical synthesis or as a research tool, although further investigation is required to fully understand its properties and uses.

126759-12-4

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126759-12-4 Usage

Uses

Used in Chemical Synthesis:
Benzamide, N-[2-methyl-1-[(propylamino)carbonyl]propyl]-3,5-dinitrois used as an intermediate compound in the synthesis of other complex molecules. Its unique structure, which includes a benzamide core and nitro groups, allows for the creation of a variety of chemical products through further reactions.
Used in Research Applications:
Benzamide, N-[2-methyl-1-[(propylamino)carbonyl]propyl]-3,5-dinitroserves as a research tool in the field of chemistry, particularly in studies focused on the properties and reactivity of nitro-containing compounds. Its complex structure provides opportunities for investigating the effects of different functional groups on chemical behavior and potential applications.
Used in Pharmaceutical Development:
Although its potential hazards must be carefully managed, Benzamide, N-[2-methyl-1-[(propylamino)carbonyl]propyl]-3,5-dinitrocould be explored for its possible pharmaceutical applications. Its structure may offer insights into the design of new drug candidates, particularly in areas where the nitro groups could play a role in biological activity.
Used in Industrial Processes:
In certain industries, Benzamide, N-[2-methyl-1-[(propylamino)carbonyl]propyl]-3,5-dinitromay be utilized in specific processes that require its unique chemical properties. Benzamide, N-[2-methyl-1-[(propylamino)carbonyl]propyl]-3,5-dinitro-'s reactivity and potential explosive nature could be harnessed in controlled environments for specific industrial applications, such as in the production of certain types of explosives or propellants, provided that safety measures are strictly adhered to.

Check Digit Verification of cas no

The CAS Registry Mumber 126759-12-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,5 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126759-12:
(8*1)+(7*2)+(6*6)+(5*7)+(4*5)+(3*9)+(2*1)+(1*2)=144
144 % 10 = 4
So 126759-12-4 is a valid CAS Registry Number.

126759-12-4SDS

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 N-[3-methyl-1-oxo-1-(propylamino)butan-2-yl]-3,5-dinitrobenzamide

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:126759-12-4 SDS

126759-12-4Relevant academic research and scientific papers

Preparation of a New Chiral Stationary Phase Based on Macrocyclic Amide Chiral Selector for the Liquid Chromatographic Chiral Separations

Sung, Ji Yeong,Choi, Seung Hyuck,Hyun, Myung Ho

, p. 253 - 258 (2016/02/26)

A new chiral stationary phase (CSP) based on macrocyclic amide receptor was prepared starting from (1R,2R)-1,2-diphenylethylenediamine. The new CSP was successfully applied to the resolution of various N-(substituted benzoyl)-α-amino amides with reasonably good separation factors and resolutions (α = 1.75 ~ 2.97 and RS = 2.89 ~ 6.82 for 16 analytes). The new CSP was also applied to the resolution of 3-substituted 1,4-benzodiazepin-2-ones and some diuretic chiral drugs including bendroflumethiazide and methylchlothiazide and metolazone. The resolution results for 3-substituted 1,4-benzodiazepin-2-ones and some diuretic chiral drugs were also reasonably good. Chirality 28:253-258, 2016.

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