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22755-34-6

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22755-34-6 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 3 carbon (C), 3 hydrogen (H), 6 nitrogen (N), and 3 bromine (Br) atoms.

Explanation

This structure indicates the arrangement of atoms in the molecule, with three nitrogen atoms (N) forming a triazine ring, and three additional nitrogen atoms (N) forming an amine group. The three bromine atoms (Br) are attached to the nitrogen atoms in the molecule.
3. Triazine derivative

Explanation

The compound is derived from the triazine ring, which is a six-membered ring containing four nitrogen atoms and two carbon atoms.
4. Flame retardant properties

Explanation

The presence of bromine atoms in the molecule provides the compound with flame-retardant properties, making it useful in various industrial and consumer products.

Explanation

Due to its flame-retardant properties, the compound is commonly used in these industries to enhance fire safety.
6. Health and environmental risks
7. Proper handling and disposal

Explanation

To minimize the health and environmental risks, it is essential to follow appropriate guidelines for handling and disposing of the compound, including using personal protective equipment and adhering to waste disposal regulations.

Chemical structure

1,3,5-Triazine-2,4,6-triamine, N2,N4,N6-tribromo-

Applications

Textiles, plastics, and electronics

Check Digit Verification of cas no

The CAS Registry Mumber 22755-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,5 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22755-34:
(7*2)+(6*2)+(5*7)+(4*5)+(3*5)+(2*3)+(1*4)=106
106 % 10 = 6
So 22755-34-6 is a valid CAS Registry Number.

22755-34-6Upstream product

22755-34-6Downstream Products

22755-34-6Relevant articles and documents

Facile one-pot synthesis of a novel series of 7-aryl-8H-benzo[h]indeno[1,2-b]quinoline-8-one derivatives catalyzed by tribromomelamine

Mansoor, Syed Sheik,Ghashang, Majid,Aswin, Krishnamoorthy

, p. 6907 - 6926 (2015/09/29)

Tribromomelamine, has been used as an efficient, inexpensive, and green catalyst for one-pot, three-component synthesis of 7-aryl-8H-benzo[h]indeno[1,2-b]quinoline-8-ones by reaction of 1,3-indanedione, aromatic aldehydes, and 1-naphthylamine under solvent-free conditions. The several advantages of this reaction include high yields, short reaction time, and high catalyst efficiency.

Trimethylsilylation of hydroxyl group with 1,1,1,3,3,3-hexamethyldisilazane (HMDS) catalyzed by tribromomelamine (TBM)

Ghorbani-Choghamarani, Arash,Zolfigol, Mohammad Ali,Hajjami, Maryam,Jafari, Shila

experimental part, p. 1208 - 1213 (2010/01/07)

Tribromomelamine (TBM) can be used as a novel catalyst for the trimethylsilylation of alcohols and phenols with 1,1,1,3,3,3- hexamethyldisilazane (HMDS). A wide variety of hydroxyl groups were selectively protected in CH2Cl2/CH3CN under mild conditions.

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