Welcome to LookChem.com Sign In|Join Free

CAS

  • or

138335-70-3

Post Buying Request

138335-70-3 Suppliers

Recommended suppliersmore

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

138335-70-3 Usage

Description

1-(2,4-dibromo-1-methyl-1H-imidazol-5-yl)-2-(6-methylpyrazin-2-yl)ethanone is an organic compound characterized by its complex molecular structure, featuring a 1H-imidazol ring with bromine and methyl substitutions at the 2nd and 4th positions, and a 6-methylpyrazin-2-yl group attached to an ethanone moiety. The presence of multiple functional groups, including halogens and heterocyclic rings, suggests that this compound may exhibit a range of chemical properties and potential applications.

Uses

Given the provided materials, the specific uses of 1-(2,4-dibromo-1-methyl-1H-imidazol-5-yl)-2-(6-methylpyrazin-2-yl)ethanone are not explicitly detailed. However, based on the structural features of the compound, we can infer potential areas of application:
Used in Pharmaceutical Industry:
1-(2,4-dibromo-1-methyl-1H-imidazol-5-yl)-2-(6-methylpyrazin-2-yl)ethanone could be used as a building block or active pharmaceutical ingredient (API) for the development of new drugs, given its complex structure and the presence of heterocyclic rings, which are common in many bioactive molecules.
Used in Chemical Synthesis:
1-(2,4-dibromo-1-methyl-1H-imidazol-5-yl)-2-(6-methylpyrazin-2-yl)ethanone may serve as an intermediate in the synthesis of other organic compounds, particularly those requiring imidazole or pyrazine moieties, due to its structural complexity and the presence of multiple functional groups.
Used in Material Science:
1-(2,4-dibromo-1-methyl-1H-imidazol-5-yl)-2-(6-methylpyrazin-2-yl)ethanone's unique structure and functional groups might endow it with specific physical or chemical properties that could be exploited in the development of new materials, such as those with specialized optical, electronic, or mechanical characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 138335-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,3 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138335-70:
(8*1)+(7*3)+(6*8)+(5*3)+(4*3)+(3*5)+(2*7)+(1*0)=133
133 % 10 = 3
So 138335-70-3 is a valid CAS Registry Number.

138335-70-3SDS

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 1-(2,5-dibromo-3-methylimidazol-4-yl)-2-(6-methylpyrazin-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 2-(6-methyl-2-pyrazinyl)-1-(2,4-dibromo-1-methyl-5-imidazolyl)ethan-1-one

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:138335-70-3 SDS

138335-70-3Relevant articles and documents

Regiospecific Synthesis of the Aminoimidazoquinoxaline (IQx) Mutagens from Cooked Foods

Bierer, Donald E.,O'Connell, John F.,Parquette, Jon R.,Thompson, Charles M.,Rapoport, Henry

, p. 1390 - 1405 (2007/10/02)

A versatile regiospecific synthesis has been developed to prepare the six dimethyl- and trimethyl-substituted 2-aminoimidazoquinoxaline (IQx) regioisomers 35, 36, 37, 38, 39, and 40 for complete and unambiguous characterization.The key reaction step in the synthetic sequence for these angular tricycles is a photodehydrohalogenative cyclization of suitably substituted pyrazinylimidazolylethylene intermediates derived from common pyrazine and fully functionalized imidazole precursors.The reaction sequence developed allows for versatility in the substitution pattern as well as total regioisomeric control for the synthesis of all possible methyl and polymethyl analogues of IQx.Comparison of the physical properties among the isomeric di- and trimethyl-IQx's has established the value of unambiguous regiospecific synthesis for structural assignments in this food mutagen series.

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

What can I do for you?
Get Best Price

Get Best Price for 138335-70-3