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143209-28-3

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143209-28-3 Usage

Chemical structure

Ethyl ester derivative of 1,2,4-triazine-5-carboxylic acid

Applications

a. Intermediate in the synthesis of pharmaceuticals
b. Intermediate in the synthesis of agrochemicals
c. Building block in the production of dyes and pigments

Solubility

Moderate solubility in water

Storage conditions

Cool, dry, and well-ventilated area

Flammability

High flammability

Safety precautions

a. Proper handling to avoid skin, eye, and respiratory irritation
b. Use of protective equipment (gloves, goggles, masks) when handling
c. Avoid exposure to high concentrations

Industrial importance

Versatile and important compound in various applications

Check Digit Verification of cas no

The CAS Registry Mumber 143209-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,0 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 143209-28:
(8*1)+(7*4)+(6*3)+(5*2)+(4*0)+(3*9)+(2*2)+(1*8)=103
103 % 10 = 3
So 143209-28-3 is a valid CAS Registry Number.

143209-28-3SDS

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 ethyl 1,2,4-triazine-5-carboxylate

1.2 Other means of identification

Product number -
Other names 1,2,4-TRIAZINE-5-CARBOXYLIC ACID,ETHYL ESTER

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:143209-28-3 SDS

143209-28-3Downstream Products

143209-28-3Relevant articles and documents

SYNTHESIS of 1,2,4-TRIAZINES - XIV. Regioselective Synthesis of Ethyl 1,2,4-Triazine-5-carboxylates

Ohsumi, Tadashi,Neunhoeffer, Hans

, p. 5227 - 5234 (2007/10/02)

Ethyl 1,2,4-triazine-5-carboxylates 6 were prepared by heating N,N-dimethylaminomethylene- or ethoxymethylenehydrazones 5 with ammonium acetate in acetic acid at 100 deg C.NMR studies confirmed the absence of their regio isomers (6-carboxylates), showing

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