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92013-92-8

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92013-92-8 Usage

General Description

2,5-Cyclohexadiene-1,4-dione, 2,3,5-trichloro-6-(4-morpholinyl)- is a chemical compound that contains a cyclohexadiene-dione ring system and three chlorine atoms. It also features a morpholinyl group, which is a six-membered heterocyclic ring containing oxygen and nitrogen atoms. 2,5-Cyclohexadiene-1,4-dione, 2,3,5-trichloro-6-(4-morpholinyl)- is used as a reagent in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is known for its ability to react with various nucleophiles and electrophiles, making it a versatile building block for creating new molecules with specific properties and functions. However, it is important to handle this compound with caution due to its potential for toxicity and environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 92013-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,1 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92013-92:
(7*9)+(6*2)+(5*0)+(4*1)+(3*3)+(2*9)+(1*2)=108
108 % 10 = 8
So 92013-92-8 is a valid CAS Registry Number.

92013-92-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5-trichloro-6-morpholin-4-ylcyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names -

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:92013-92-8 SDS

92013-92-8Downstream Products

92013-92-8Relevant articles and documents

SPECTROPHOTOMETRIC DETERMINATION OF AMINES WITH P-CHLORANIL.

Smith,Davis

, p. 2345 - 2349 (2007/10/02)

Primary, secondary, and tertiary amines, both aliphatic and aromatic are shown to react with p-chloranil in dioxane/2-propanol (1:4, v/v) to produce a blue to purple color. Most amines tested also react with p-chloranil in other organic solvents. The colored compound formed can be stable for 8 h at room temperature, depending on the amine and the solvent used. Several organic compounds (phenol, epoxies, alkynes, and non-amine nitrogens) are shown to not interfere with the detemination of amines. A few applications of amine determinations in real samples are discussed.

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