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[2-[[4-(aminosulphonyl)phenyl]amino]-1,4-dihydro-4-oxo-5-pyrimidinyl]carbamoyl chloride is a chemical compound characterized by its molecular formula C11H11ClN6O4S. It is a carbamoyl chloride derivative featuring a pyrimidine ring and an aminosulphonylphenyl group, which contributes to its versatile applications in various fields.

89074-09-9

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89074-09-9 Usage

Uses

Used in Pharmaceutical Synthesis:
[2-[[4-(aminosulphonyl)phenyl]amino]-1,4-dihydro-4-oxo-5-pyrimidinyl]carbamoyl chloride is used as a building block for the synthesis of pharmaceuticals. Its unique chemical structure allows it to be a key component in the development of new drug molecules.
Used in Agrochemical Production:
In the agrochemical industry, [2-[[4-(aminosulphonyl)phenyl]amino]-1,4-dihydro-4-oxo-5-pyrimidinyl]carbamoyl chloride is used as a starting material for the creation of various agrochemicals, such as pesticides and herbicides, due to its antimicrobial properties.
Used in Antimicrobial Applications:
[2-[[4-(aminosulphonyl)phenyl]amino]-1,4-dihydro-4-oxo-5-pyrimidinyl]carbamoyl chloride is utilized as an antimicrobial agent, providing protection against a range of microorganisms, including bacteria and fungi. Its effectiveness in inhibiting microbial growth makes it a valuable asset in the development of antimicrobial products.
Used in Antitumor Applications:
[2-[[4-(aminosulphonyl)phenyl]amino]-1,4-dihydro-4-oxo-5-pyrimidinyl]carbamoyl chloride is also recognized for its antitumor properties, making it a potential candidate for the development of cancer treatments. Its ability to target and inhibit tumor growth could lead to novel therapeutic approaches in oncology.
Used in Medical Imaging:
Furthermore, [2-[[4-(aminosulphonyl)phenyl]amino]-1,4-dihydro-4-oxo-5-pyrimidinyl]carbamoyl chloride has the potential to be used as a diagnostic tool in medical imaging applications. Its unique chemical properties may allow for the enhancement of imaging techniques, leading to improved detection and monitoring of various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 89074-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,7 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89074-09:
(7*8)+(6*9)+(5*0)+(4*7)+(3*4)+(2*0)+(1*9)=159
159 % 10 = 9
So 89074-09-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H10ClN5O4S/c12-10(19)16-8-5-14-11(17-9(8)18)15-6-1-3-7(4-2-6)22(13,20)21/h1-5H,(H,16,19)(H2,13,20,21)(H2,14,15,17,18)

89074-09-9SDS

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 N-[6-oxo-2-(4-sulfamoylanilino)-1H-pyrimidin-5-yl]carbamoyl chloride

1.2 Other means of identification

Product number -
Other names 2-(p-aminosulfonyl)anilino-5-chlorocarbonylamino-4-hydroxy-pyrimidine

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:89074-09-9 SDS

89074-09-9Relevant academic research and scientific papers

Synthesis and antibacterial activity of pyrimidinylureidopenicillins

Wetzel,Woitun,Reuter,Maier,Lechner

, p. 343 - 348 (2007/10/02)

The 6R-[(R)-2-[3-[5-pyrimidinyl]ureido]-2-(4-hydroxyphenyl)acetamido]-penicill anic acids, prepared by two synthetic routes, exhibit broad antimicrobial activity against Gram-positive and Gram-negative bacteria. Their structure-activity relationships are discussed. 6R-[(R)-2-[3-[2-(p-aminosulfonyl)anilino-4-hydroxy-5-pyrimidinyl]ureido]-2 -(4-hydroxyphenyl)acetamido]-penicillanic acid, sodium salt (VX-VC 43), the most active compound, shows very low MIC (minimal inhibitory concentration) values against clinically important Gram-negative bacteria, primarily Pseudomonas aeruginosa.

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