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187235-49-0

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187235-49-0 Usage

Description

(6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-yl (4-bromophenyl)carbamate is a complex organic molecule characterized by its unique fused ring structure, which includes an imidazole ring and an oxazine ring. (6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-yl (4-bromophenyl)carbamate also features a nitro group and a carbamate functional group, along with a 4-bromophenyl group, indicating the presence of a benzene ring substituted with a bromine atom. The specific arrangement of these functional groups and the stereochemistry of the molecule at the 6S position are likely to contribute to its potential biological activity or chemical reactivity. (6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-yl (4-bromophenyl)carbamate may find applications in various fields, such as medicinal chemistry and material science, due to its distinct chemical structure.

Uses

Used in Medicinal Chemistry:
(6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-yl (4-bromophenyl)carbamate is used as a potential pharmaceutical compound for its possible biological activity. The unique arrangement of functional groups and the stereochemistry at the 6S position may provide specific interactions with biological targets, making it a candidate for drug development.
Used in Material Science:
In the field of material science, (6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-yl (4-bromophenyl)carbamate may be utilized for the development of novel materials with specific properties. (6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-yl (4-bromophenyl)carbamate's chemical structure, including the fused rings and functional groups, could contribute to the creation of materials with tailored characteristics for various applications.
Used in Chemical Research:
(6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-yl (4-bromophenyl)carbamate serves as a subject of interest in chemical research. Its complex structure and potential reactivity make it a valuable compound for studying reaction mechanisms, exploring new synthetic routes, and understanding the relationship between chemical structure and biological activity.
Used in Drug Design and Development:
(6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-yl (4-bromophenyl)carbamate is used as a lead molecule in drug design and development. Its unique chemical structure and potential biological activity make it a promising candidate for further optimization and development into a therapeutic agent targeting specific diseases or conditions.
Used in Chemical Synthesis:
(6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-yl (4-bromophenyl)carbamate may be employed as an intermediate or building block in the synthesis of more complex molecules. Its functional groups and structural features can be exploited to create a variety of novel compounds with potential applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 187235-49-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,2,3 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 187235-49:
(8*1)+(7*8)+(6*7)+(5*2)+(4*3)+(3*5)+(2*4)+(1*9)=160
160 % 10 = 0
So 187235-49-0 is a valid CAS Registry Number.

187235-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-yl (4-bromophenyl)carbamate

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 -
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More Details:187235-49-0 SDS

187235-49-0Relevant articles and documents

Structure-activity relationships for amide-, carbamate-, and urea-linked analogues of the tuberculosis drug (6S)-2-nitro-6-{[4-(trifluoromethoxy)benzyl] oxy}-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine (PA-824)

Blaser, Adrian,Palmer, Brian D.,Sutherland, Hamish S.,Kmentova, Iveta,Franzblau, Scott G.,Wan, Baojie,Wang, Yuehong,Ma, Zhenkun,Thompson, Andrew M.,Denny, William A.

supporting information; experimental part, p. 312 - 326 (2012/03/07)

Analogues of clinical tuberculosis drug (6S)-2-nitro-6-{[4- (trifluoromethoxy)benzyl]oxy}-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine (PA-824), in which the OCH2 linkage was replaced with amide, carbamate, and urea functionality, were investigate

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