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4-(5-bromopyrimidin-2-yloxy)benzenamine is a complex organic chemical compound characterized by the molecular formula C11H8BrN3O. It features a benzene ring connected to an amine group and a pyrimidine ring, which is substituted with a bromine atom. 4-(5-bromopyrimidin-2-yloxy)benzenamine holds potential in the fields of medicinal chemistry and drug development due to its unique structural attributes, which may allow it to serve as a precursor in the synthesis of biologically active molecules or pharmaceuticals.

76660-37-2

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76660-37-2 Usage

Uses

Used in Medicinal Chemistry:
4-(5-bromopyrimidin-2-yloxy)benzenamine is used as a building block in the synthesis of biologically active molecules for medicinal chemistry. Its structural features make it a promising candidate for the development of new pharmaceuticals.
Used in Drug Development:
In the pharmaceutical industry, 4-(5-bromopyrimidin-2-yloxy)benzenamine is utilized as a key intermediate in the creation of novel drugs. Its potential applications in drug development hinge on further research and testing to explore its specific properties and therapeutic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 76660-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,6 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76660-37:
(7*7)+(6*6)+(5*6)+(4*6)+(3*0)+(2*3)+(1*7)=152
152 % 10 = 2
So 76660-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H8BrN3O/c11-7-5-13-10(14-6-7)15-9-3-1-8(12)2-4-9/h1-6H,12H2

76660-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(5-bromopyrimidin-2-yl)oxyaniline

1.2 Other means of identification

Product number -
Other names 4-(5-Bromopyrimidin-2-yloxy)phenylamine

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:76660-37-2 SDS

76660-37-2Downstream Products

76660-37-2Relevant academic research and scientific papers

hTERT MODULATORS AND METHODS OF USE

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Paragraph 0093; 0094; 0095; 0111, (2018/02/28)

The present invention provides hTERT modulators and methods for producing and using the same. In particular, the present invention provide a compound of the formula as described herein. Some aspects of the invention are based on the characterization of the effect of hTERT core promoter region mutants on the 5-12 G-quadruplex structure and its stability. It is believed that some of the compounds of the invention bind selectively to the G-quadruplex in the hTERT core promoter mutant, which results in reversal of the effect of mutant promoter activation.

Aryloxy anilino propionic ester compound and application thereof as herbicide

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, (2016/10/09)

An aryloxy anilino propionic ester compound comprises the structure shown in the general formula (I), wherein Ar is aromatic heterocycle or fused heterocycle. Please see the specification for the chemical formula of the aromatic heterocycle and the chemical formula of the fused heterocycle, wherein R1, R2, R3 and R4 are one or more of H, halogen, nitro, methoxy group, methyl, methyl formate group, cyanogroup and trihalomethyl, R5 is the alkyl group on the linear chain or branched chain of H and C1-C4, hydrogen on the alkyl group is substituted by hydroxyl, carboxyl, mercapto group, amino, guanidyl and phenyl, and R6 is one of methyl, ethyl, butyl and the substance specified in the specification. The compound has the advantages that the characteristics of being efficient, capable of acting quickly and not prone to resistance generation of (aryloxy) phenoxypropionate herbicides can be maintained, amino acid functional groups in molecules can be designed to serve as adulterate amino acid so as to restrain the biosynthesis of protein of plants, and all weeds can be controlled.

Benzoylphenylurea sulfur analogues with potent antitumor activity

Hallur, Gurulingappa,Jimeno, Antonio,Dalrymple, Susan,Zhu, Tao,Jung, M. Katherine,Hidalgo, Manuel,Isaacs, John T.,Sukumar, Saraswati,Hamel, Ernest,Khan, Saeed R.

, p. 2357 - 2360 (2007/10/03)

A novel series of BPU analogues were synthesized and evaluated for antitumor activity. In particular, BPU sulfur analogues 6n and 7d were shown to possess up to 10-fold increased potency, when compared to 1 (NSC-639829), against cancer cell lines. 6n was

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