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141602-25-7

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141602-25-7 Usage

General Description

Pyrimidine, 4-chloro-6-ethyl- (9CI) is a chemical compound with the molecular formula C6H6ClN2. It is a member of the pyrimidine family, which are heterocyclic organic compounds that contain a ring structure with two nitrogen atoms. This particular derivative is characterized by the presence of a 4-chloro-6-ethyl group, which adds specific chemical properties to the molecule. It may be used in various research and industrial applications, including as a building block in the synthesis of pharmaceuticals and agrochemicals. Additionally, its structural features make it a potentially interesting target for further investigation in the field of medicinal chemistry. Overall, the compound has potential relevance in the development of new drugs and chemical products due to its specific structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 141602-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,6,0 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141602-25:
(8*1)+(7*4)+(6*1)+(5*6)+(4*0)+(3*2)+(2*2)+(1*5)=87
87 % 10 = 7
So 141602-25-7 is a valid CAS Registry Number.

141602-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-6-ethylpyrimidine

1.2 Other means of identification

Product number -
Other names 4-chloranyl-6-ethyl-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:141602-25-7 SDS

141602-25-7Relevant articles and documents

Synthesis method of voriconazole impurity B

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Paragraph 0028-0029, (2019/10/23)

The invention relates to a synthesis method of a voriconazole impurity B. The synthesis method of the voriconazole impurity B comprises the steps of firstly, dissolving formamidine acetate and sodiumtert-butoxide in methyl alcohol, conducting stirring und

Preparation of triazoles by organometallic addition to ketones and intermediates therefor

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, (2008/06/13)

A process for the preparation of a compound of the formula: or an acid addition or base salt thereof, wherein R is phenyl optionally substituted by 1 to 3 substituents each independently selected from halo and trifluoromethyl; R1 is C1-C6 alkyl; and “Het” is pyrimidinyl optionally substituted by 1 to 3 substituents each independently selected from C1-C4 alkyl, C1-C4 alkoxy, halo, oxo, benzyl and benzyloxy, comprising reacting a compound of the formula: with a compound of the formula wherein X is chloro, bromo or iodo, the reaction taking place in the presence of zinc; at least one of iodine or a Lewis acid; and an aprotic organic solvent: optionally further reacting the resulting compound with an acid or base to form the corresponding acid addition or base salt thereof.

Aryl group- or aromatic heterocyclic group-substituted aminoquinolone derivatives and anti-HIV agent

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, (2008/06/13)

Disclosed are an aryl group- or heterocyclic group-substituted aminoquinolone compound represented by the formula (Ia), (Ib) or (Ic): STR1 wherein each of the substitutents are defined in the specification, or a salt of the compound, and an AIDS curing agent containing the same as an effective ingredient.

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