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Bromebric acid, a chemical compound with antineoplastic properties, is utilized as a reactant in the preparation of antitumor agents. It possesses the ability to inhibit the growth and progression of cancer cells, making it a valuable component in the development of cancer treatments.

16170-76-6

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16170-76-6 Usage

Uses

Used in Pharmaceutical Industry:
Bromebric acid is used as a reactant for the preparation of antitumor agents, specifically due to its antineoplastic activity. This activity allows it to contribute to the development of medications that target and combat cancer cells.
Additionally, bromebric acid may be employed in other industries where its antineoplastic properties can be leveraged for specific applications, such as in the development of targeted drug delivery systems or as a component in the synthesis of novel cancer-fighting compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 16170-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,7 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16170-76:
(7*1)+(6*6)+(5*1)+(4*7)+(3*0)+(2*7)+(1*6)=96
96 % 10 = 6
So 16170-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H9BrO4/c1-16-8-4-2-7(3-5-8)11(15)9(12)6-10(13)14/h2-6H,1H3,(H,13,14)/b9-6+

16170-76-6SDS

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 bromebric acid

1.2 Other means of identification

Product number -
Other names 3-p-Anisoyl-3-bromacrylsaeure

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:16170-76-6 SDS

16170-76-6Relevant academic research and scientific papers

Pyridazines. XV. Synthesis of 6-aryl-5-amino-3(2H)-pyridazinones as potential platelet aggregation inhibitors

Estevez, Isabel,Ravina, Enrique,Sotelo, Eddy

, p. 1421 - 1428 (2007/10/03)

Several 3(2H)-pyridazinones with amino groups at the 5-position of the pyridazine nucleus have been prepared. The 6-aryl-5-halo-3(2H)-pyridazinones obtained from mucochloric and mucobromic acid lead to the corresponding 5- alkylamino-3(2H)-pyridazinones,

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