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(3-Bromo-5-nitrophenyl)(pyrrolidin-1-yl)methanone is a chemical compound characterized by the molecular formula C12H12BrN2O3. It is a yellow crystalline solid that features a bromine and a nitro group attached to a phenyl ring, along with a pyrrolidine ring. (3-Bromo-5-nitrophenyl)(pyrrolidin-1-yl)methanone is utilized in organic synthesis and pharmaceutical research, making it a valuable asset to researchers and chemists in the field of organic chemistry.

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  • 941294-20-8 Structure
  • Basic information

    1. Product Name: (3-Bromo-5-nitrophenyl)(pyrrolidin-1-yl)methanone
    2. Synonyms: (3-Bromo-5-nitrophenyl)(pyrrolidin-1-yl)methanone;1-(3-Bromo-5-nitrobenzoyl)pyrrolidine97%
    3. CAS NO:941294-20-8
    4. Molecular Formula: C11H11BrN2O3
    5. Molecular Weight: 299.12
    6. EINECS: N/A
    7. Product Categories: blocks;Bromides;Carboxes;NitroCompounds
    8. Mol File: 941294-20-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: (3-Bromo-5-nitrophenyl)(pyrrolidin-1-yl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-Bromo-5-nitrophenyl)(pyrrolidin-1-yl)methanone(941294-20-8)
    11. EPA Substance Registry System: (3-Bromo-5-nitrophenyl)(pyrrolidin-1-yl)methanone(941294-20-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 941294-20-8(Hazardous Substances Data)

941294-20-8 Usage

Uses

Used in Organic Synthesis:
(3-Bromo-5-nitrophenyl)(pyrrolidin-1-yl)methanone is used as a reagent in the preparation of various organic compounds. Its unique structure allows for versatile reactions and the synthesis of a wide range of chemical products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3-Bromo-5-nitrophenyl)(pyrrolidin-1-yl)methanone is being investigated for its potential pharmacological properties. Its presence in the development of new drugs and therapeutic agents highlights its importance in advancing medical treatments.
Used in Research and Development:
(3-Bromo-5-nitrophenyl)(pyrrolidin-1-yl)methanone is also utilized in research and development settings, where its unique structure and properties are explored for new applications and insights into organic chemistry. This includes the study of its reactivity, stability, and potential interactions with other compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 941294-20-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,1,2,9 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 941294-20:
(8*9)+(7*4)+(6*1)+(5*2)+(4*9)+(3*4)+(2*2)+(1*0)=168
168 % 10 = 8
So 941294-20-8 is a valid CAS Registry Number.

941294-20-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-Bromo-5-nitrophenyl)(pyrrolidin-1-yl)methanone

1.2 Other means of identification

Product number -
Other names (3-bromo-5-nitrophenyl)-pyrrolidin-1-ylmethanone

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:941294-20-8 SDS

941294-20-8Relevant articles and documents

FUSED PYRAZINE DERIVATIVES AS KINASE INHIBITORS

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Page/Page column 47, (2010/06/11)

A series of quinoxaline derivatives, and analogues thereof, which are functionalised further by a substituted phenyl or pyridinyl moiety, being selective inhibitors of PO kinase enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, oncological, nociceptive or ophthalmic conditions.

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