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5725-46-2

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5725-46-2 Usage

Appearance

White, crystalline solid

Taste

Slightly sweet

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Antimicrobial properties

Effective against various microorganisms

Antioxidant properties

Helps prevent oxidation and spoilage in products

Application in personal care and cosmetic products

Valuable ingredient due to its antimicrobial and antioxidant properties

Potential as a corrosion inhibitor

Used in metalworking fluids to prevent corrosion

Component in flame-retardant materials

Enhances fire resistance in various materials

Check Digit Verification of cas no

The CAS Registry Mumber 5725-46-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,2 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5725-46:
(6*5)+(5*7)+(4*2)+(3*5)+(2*4)+(1*6)=102
102 % 10 = 2
So 5725-46-2 is a valid CAS Registry Number.

5725-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-1,3,5-triazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names 2,4,6-trioxo-1-phenylhexahydro-1,3,5-triazin

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:5725-46-2 SDS

5725-46-2Relevant articles and documents

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Close

, p. 3617,3618 (1953)

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About the Preparation and Chlorination of Carbonyl Diisothiocyanate

Bunnenberg, Rolf,Jochims, Johannes C.,Haerle, Helmut

, p. 3587 - 3596 (2007/10/02)

An improved preparation of carbonyl diisothiocyanate (1) is described.Compound 1 can be stored in form of its stable hydrochloride 3.Depending on the reaction conditions chlorination of 1 leads to the acyl isocyanide dichlorides 5 or 8.Compound 5 reacts with amines to give: the triazines 9a - c, the ammelines 11a, b, the guanidines 12 and 16a, or the acylcarbodiimides 14 and 15.With sodium phenolate 5 forms the dialkylidene urea 17, and with thiolates the derivatives 18a - c of dithiocarbonic acid.Compound 8 racts with thiophenolate to give 19 and with tert-butylamine to yield the carbamoylcarbodiimide 20.

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