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4-Quinazolinecarboxylic acid, 6-bromo-, ammonium salt is a quinazoline derivative with the molecular formula C9H8BrN3O2. It features a carboxylic acid group and a bromine atom at the 6 position, and is typically found as an ammonium salt, which enhances its stability and solubility in water. 4-Quinazolinecarboxylic acid, 6-bromo-, ammonium salt is a valuable intermediate in organic synthesis and drug development due to its unique structure and properties.

474710-80-0

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474710-80-0 Usage

Uses

Used in Pharmaceutical Industry:
4-Quinazolinecarboxylic acid, 6-bromo-, ammonium salt is used as a building block for the synthesis of various biologically active compounds, including potential drug candidates. Its unique structure and properties make it a valuable intermediate in the development of new pharmaceuticals.
Used in Organic Synthesis:
4-Quinazolinecarboxylic acid, 6-bromo-, ammonium salt is utilized as an intermediate in organic synthesis, where its quinazoline core and functional groups can be further modified to create a variety of chemical entities with different biological activities and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 474710-80-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,7,1 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 474710-80:
(8*4)+(7*7)+(6*4)+(5*7)+(4*1)+(3*0)+(2*8)+(1*0)=160
160 % 10 = 0
So 474710-80-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H5BrN2O2/c10-5-1-2-7-6(3-5)8(9(13)14)12-4-11-7/h1-4H,(H,13,14)

474710-80-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ammonium 6-bromoquinazoline-4-carboxylate

1.2 Other means of identification

Product number -
Other names azanium,6-bromoquinazoline-4-carboxylate

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:474710-80-0 SDS

474710-80-0Upstream product

474710-80-0Relevant academic research and scientific papers

NITROGENOUS FUSED?RING COMPOUND HAVING PYRAZOLYL GROUP AS SUBSTITUENT AND MEDICINAL COMPOSITION THEREOF

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Page 198; 199, (2008/06/13)

The present invention provides a compound having an excellent inhibitory action on activation of STAT6 and a pharmaceutical composition thereof. Inparticular, it provides a compound represented by the following formula (I), a salt thereof or a hydrate of them. In the formula, X represents a nitrogen-containing condensed aromatic heterocyclic group such as imidazo[1,2-a]pyridine, benzimidazole, quinazoline, quinoline, or 2,1-benzisoxazole and has (R4)n as substituent groups; Y represents a C3-8 cycloalkyl group, C4-8 cycloalkenyl group, 5- to 14-membered non-aromatic heterocyclic group, C6-14 aromatic hydrocarbon cyclic group or 5- to 14-membered aromatic heterocyclic group; n in (R4)n is 0, 1, 2 or 3, and Z groups independently represent (1) hydrogen atom, (2) amino group, (3) halogen atom, (4) hydroxyl group, (5) nitro group, (6) cyano group, (7) azido group, (8) formyl group, (9) hydroxyamino group, (10) sulfamoyl group, (11) guanodino group, (12) oxo group, (13) C2-6 alkenyl group, (14) C1-6 alkoxy group, (15) C1-6 alkylhydroxyamino group, (16) halogenated C1-6 alkyl group, (17) halogenated C2-6 alkenyl group, (18) (i) C3-7cycloalkyl group, (ii) C3-7cycloalkenyl group, (iii) 5- to 14-membered non-aromatic heterocyclic group, each of which may have one or more substituent groups Q, or (19) formula -M1-M2-M3, R1 represents (1) hydrogen atom, (2) halogen atom, (3) hydroxyl group, (4) nitro group, (5) cyano group, (6) halogenated C1-6 alkyl group, (7) C2-6 alkyl group substituted with a hydroxyl or cyano group, (8) C2-6 alkenyl group, or (9) formula -L1-L2-L3, and R2 represents a hydrogen atom or a protecting group; and R3 represents a hydrogen atom, halogen atom, cyano group, amino group, C1-4 alkyl group or halogenated C1-4 alkyl group.

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