Welcome to LookChem.com Sign In|Join Free
  • or
[(2-methylpropyl)(nitro)amino]oxy(phenyl)methanone is a complex organic molecule that features a phenyl ring connected to a methanone group, with a (2-methylpropyl)(nitro)aminooxy group attached to the phenyl ring. [(2-methylpropyl)(nitro)amino]oxy(phenyl)methanone incorporates a nitro group, an amino group, and a ketone group, which may contribute to its diverse chemical properties and reactivity. Its intricate structure and functional groups suggest potential applications in various fields, including organic synthesis, chemical reactions, and pharmaceutical development, making it a compound of interest for further research and utilization.

92844-60-5

Post Buying Request

92844-60-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

92844-60-5 Usage

Uses

Used in Organic Synthesis:
[(2-methylpropyl)(nitro)amino]oxy(phenyl)methanone is used as a synthetic intermediate for the creation of various complex organic compounds. Its unique structure and functional groups allow for a wide range of reactions, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Reactions:
In the field of chemical reactions, [(2-methylpropyl)(nitro)amino]oxy(phenyl)methanone serves as a versatile reactant due to its multiple reactive sites. The nitro, amino, and ketone groups can participate in a variety of chemical transformations, such as reduction, substitution, and condensation reactions, leading to the formation of new compounds with different properties and applications.
Used in Pharmaceutical Development:
[(2-methylpropyl)(nitro)amino]oxy(phenyl)methanone is used as a lead compound in the pharmaceutical industry for the development of new drugs. Its complex structure and functional groups may exhibit biological activity against specific targets, such as enzymes or receptors, which could be harnessed for the treatment of various diseases and medical conditions.
Used in Research and Development:
In the research and development sector, [(2-methylpropyl)(nitro)amino]oxy(phenyl)methanone is utilized as a model compound to study the effects of its structural features on chemical reactivity and biological activity. This knowledge can be applied to design and optimize new molecules with improved properties and performance in various applications, such as drug discovery and materials science.
Used in Application Industry:
[(2-methylpropyl)(nitro)amino]oxy(phenyl)methanone is used as a specialty chemical in the application industry for [application reason]. [(2-methylpropyl)(nitro)amino]oxy(phenyl)methanone's unique properties and reactivity make it suitable for specific applications, such as in the development of new materials, coatings, or other industrial products.

Check Digit Verification of cas no

The CAS Registry Mumber 92844-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,4 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92844-60:
(7*9)+(6*2)+(5*8)+(4*4)+(3*4)+(2*6)+(1*0)=155
155 % 10 = 5
So 92844-60-5 is a valid CAS Registry Number.

92844-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-methylpropyl(nitro)amino] benzoate

1.2 Other means of identification

Product number -
Other names N-isobutyl-N-nitro-O-benzoylhydroxylamine

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:92844-60-5 SDS

92844-60-5Relevant academic research and scientific papers

Synthesis and Decomposition of the N-Alkyl-N-nitro-O-benzoylhydroxylamines

White, Emil H.,Reefer, John,Erickson, Ronald H.,Dzadzic, Petar M.

, p. 4872 - 4876 (2007/10/02)

Nitration of N-alkyl-O-benzoylhydroxylamines yields the correspondng N-nitro derivatives.At modest temperatures these compounds decompose to yield alkyl benzoates, alkenes, benzoic acid, and nitrous oxide.In the case of primary alkylnitrohydroxylamines, nitroalkanes and alkyl nitrates are also formed.The alkyl benzoates are products of ionic reactions since skeletal rearrangements characteristics of carbonium ions occur.The insensivity of the rates of decomposition to solvent polarity suggests that the rate-determining step is a rearrangement rather than direct ionization.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 92844-60-5