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5-(benzyloxy)-2,4-dichloropyrimidine is a chemical compound with the molecular formula C13H10Cl2N2O. It is a white to off-white crystalline powder that is sparingly soluble in water but more soluble in organic solvents. 5-(benzyloxy)-2,4-dichloropyrimidine belongs to the class of pyrimidine derivatives and is used in various chemical and pharmaceutical applications. It is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. With potential applications in the development of new drugs, 5-(benzyloxy)-2,4-dichloropyrimidine serves as a building block in organic synthesis. Proper care and adherence to safety guidelines are essential when handling 5-(benzyloxy)-2,4-dichloropyrimidine to avoid potential health hazards.

91183-17-4

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91183-17-4 Usage

Uses

Used in Pharmaceutical Industry:
5-(benzyloxy)-2,4-dichloropyrimidine is used as an intermediate in the synthesis of pharmaceuticals for its potential applications in the development of new drugs. Its unique chemical structure allows it to be a valuable building block in the creation of various medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 5-(benzyloxy)-2,4-dichloropyrimidine is utilized as an intermediate in the synthesis of agrochemicals, contributing to the development of effective and innovative products for agricultural applications.
Used in Organic Synthesis:
5-(benzyloxy)-2,4-dichloropyrimidine is employed as a building block in organic synthesis, enabling the creation of a wide range of organic compounds for various applications across different industries. Its versatility and reactivity make it a valuable component in the synthesis process.
Used in Research and Development:
5-(benzyloxy)-2,4-dichloropyrimidine is also used in research and development settings, where it can be explored for its potential applications in creating new chemical entities and understanding its properties and reactions with other compounds.
It is crucial to handle 5-(benzyloxy)-2,4-dichloropyrimidine with proper care and follow safety guidelines to minimize any health risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 91183-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,8 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91183-17:
(7*9)+(6*1)+(5*1)+(4*8)+(3*3)+(2*1)+(1*7)=124
124 % 10 = 4
So 91183-17-4 is a valid CAS Registry Number.
InChI:InChI=1S/C11H8Cl2N2O/c12-10-9(6-14-11(13)15-10)16-7-8-4-2-1-3-5-8/h1-6H,7H2

91183-17-4SDS

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 5-(Benzyloxy)-2,4-dichloropyrimidine

1.2 Other means of identification

Product number -
Other names 2,4-dichloro-5-phenylmethoxypyrimidine

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:91183-17-4 SDS

91183-17-4Relevant academic research and scientific papers

4-SUBSTITUTED-(3-SUBSTITUTED-1H-PYRAZOLE-5-AMINO)-PYRIMIDINE DERIVATIVES HAVING ACTIVITY OF INHIBITING PROTEIN KINASE AND USE THEREOF

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Paragraph 0168; 0173; 0174, (2014/07/23)

Provided are derivatives substituted by urea associated with 4-substituted-(3-substituted-1H-pyrazole-5-amino)-pyrimidine-2-amino of formula (I), wherein these compounds may selectively regulate or inhibit an information transmission process controlled by

4-SUBSTITUTED-(3-SUBSTITUTED-1H-PYRAZOLE-5-AMINO)-PYRIMIDINE DERIVATIVES HAVING ACTIVITY OF INHIBITING PROTEIN KINASE AND USE THEREOF

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Paragraph 0380; 0385; 0386, (2015/01/07)

Provided are derivatives substituted by urea associated with 4-substituted-(3-substituted-1H-pyrazole-5-amino)-pyrimidine-2-amino of formula (I), wherein these compounds may selectively regulate or inhibit an information transmission process controlled by

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