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16370-63-1

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16370-63-1 Usage

Description

2-Amino-4,6-dimethoxy-1,3,5-triazine, also known as Amino-Triazine, is a versatile chemical compound with the molecular formula C5H9N3O3. It is a white crystalline solid that exhibits solubility in both water and organic solvents. Characterized by its ability to react with a variety of functional groups, Amino-Triazine is widely recognized for its applications across different industries, including pharmaceuticals, agrochemicals, dyes, polymers, resins, flame retardants, antioxidants, and corrosion inhibitors. Its favorable toxicological profile further enhances its utility in these fields.

Uses

Used in Pharmaceutical Industry:
2-Amino-4,6-dimethoxy-1,3,5-triazine is used as a building block for the synthesis of various pharmaceuticals due to its reactivity with multiple functional groups, enabling the creation of a broad spectrum of medicinal compounds.
Used in Agrochemical Industry:
In agrochemicals, 2-Amino-4,6-dimethoxy-1,3,5-triazine serves as a key component in the development of pesticides and other agricultural chemicals, contributing to crop protection and yield enhancement.
Used in Dye Industry:
Amino-Triazine is utilized as a starting material in the production of dyes, where its chemical properties allow for the creation of a diverse range of colorants for various applications.
Used in Polymer and Resin Production:
2-Amino-4,6-dimethoxy-1,3,5-triazine acts as a cross-linking agent in the manufacturing of polymers and resins, improving the structural integrity and performance of these materials.
Used in Flame Retardant Manufacturing:
2-AMINO-4,6-DIMETHOXY-1,3,5-TRIAZINE is used as a component in flame retardants, enhancing the fire resistance of various materials and contributing to safety in different applications.
Used in Antioxidant and Corrosion Inhibitor Production:
Amino-Triazine is incorporated into the production of antioxidants and corrosion inhibitors, where it helps to prevent degradation and corrosion in materials, extending their lifespan and improving performance.

Check Digit Verification of cas no

The CAS Registry Mumber 16370-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,7 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16370-63:
(7*1)+(6*6)+(5*3)+(4*7)+(3*0)+(2*6)+(1*3)=101
101 % 10 = 1
So 16370-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N4O2/c1-10-4-7-3(6)8-5(9-4)11-2/h1-2H3,(H2,6,7,8,9)

16370-63-1SDS

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 2-Amino-4,6-Dimethoxy-1,3,5-Triazine

1.2 Other means of identification

Product number -
Other names 2-Amino-4,6-dimethoxy-1,3,5-triazine

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:16370-63-1 SDS

16370-63-1Relevant articles and documents

Synthesis of o-(2-Indolyl)benzoic Acids from Indole

Itahara, Toshio

, p. 305 - 306 (1981)

Treatment of 6H-isoindoloindol-6-ones with potassium t-butoxide/t-butyl alcohol containing a small amount of water at 82 deg C afforded o-(2-indolyl)benzoic acids in good yields.

Simulated sunlight-induced photodegradations of triasulfuron and cinosulfuron in aqueous solutions

Vulliet,Emmelin,Grenier-Loustallot,Paisse,Chovelon

, p. 1081 - 1088 (2007/10/03)

To elucidate the photochemical behavior of two sulfonylureas (cinosulfuron and triasulfuron) for which the chemical formulas are relatively close, their photodegradation was studied in water. All experiments were carried out under laboratory conditions using a xenon arc lamp as the source of radiation to simulate environmental conditions. Polychromatic quantum efficiencies were calculated to determine the photochemical pesticide lifetimes at pH 7, and a comparison with hydrolysis lifetimes has been performed. The results obtained showed clearly that at pH 7, photodegradation becomes a more important pathway than chemical degradation. HPLC-DAD was used to study the kinetics for both sulfonylureas and their photoproducts, whereas HPLC-MS (ESI in positive and negative modes) was used to identify photoproducts. These results suggest that the photodegradation of these two sulfonylureas proceeds via a number of reaction pathways: (1) cleavage of the sulfonylurea bridge; (2) desulfonylation, which can proceed either by a carbon-sulfur cleavage or a nitrogen-sulfur cleavage; (3) O-demethylation of methoxy moieties present on the triazine ring; and (4) O-dealkylation of benzene derivatives. In addition, it was found that the desulfonylation represented the main step and that it was wavelength dependent.

Process for producing sulfonylureas

-

, (2008/06/13)

There is described a novel process for producing sulfonylureas of formula I STR1 wherein R1 is hydrogen or alkyl, R2 is STR2 E is =N-- or =CH--, R3 is alkyl, alkoxy or halogen, R4 is alkyl, cycloalkyl, alkoxy, halogen, alkoxy-alkyl, halo-alkyl or halo-alkoxy, R5 is hydrogen or alkyl, T is a substituted phenyl group STR3 Y is hydrogen or halogen, X is hydrogen, halogen, alkyl, halo-alkyl, alkenyl, halo-alkenyl, alkynyl, alkoxy, halo-alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, halo-alkylthio, alkylsulfonyloxy, phenylsulfonyloxy, phenylsulfonyloxy mono- or polysubstituted by alkyl, or is di-alkylsulfamoyl, and A is a bridge member which has 3 or 4 atoms and which contains 1 or 2 hetero atoms, selected from the group consisting of oxygen, sulfur and nitrogen, the said process comprising reacting a silfonamide of the formula II in the presence of a base, with diphenyl carbonate to form a salt of a phenyl carbamate converting this salt into the free phenyl carbamate and reacting this further with an amine. Sulfonylureas are herbicidally effective compounds.

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