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16584-00-2

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16584-00-2 Usage

General Description

2-Methyl-2H-benzotriazole is a chemical compound belonging to the class of benzotriazoles, which are widely used as corrosion inhibitors and UV absorbers in the synthesis of plastics, rubbers, and coatings. It is also employed as a stabilizer for the protection of metals and serves as an anticorrosive agent in industrial and commercial products. Furthermore, 2-Methyl-2H-benzotriazole exhibits potential environmental toxicity and is categorized as a hazardous chemical. Its molecular structure and properties make it suitable for various industrial applications, particularly for preserving the integrity and durability of materials exposed to harsh conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 16584-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,8 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16584-00:
(7*1)+(6*6)+(5*5)+(4*8)+(3*4)+(2*0)+(1*0)=112
112 % 10 = 2
So 16584-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3/c1-10-8-6-4-2-3-5-7(6)9-10/h2-5H,1H3

16584-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylbenzotriazole

1.2 Other means of identification

Product number -
Other names 2-Methyl-2H-benzotriazol

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:16584-00-2 SDS

16584-00-2Relevant articles and documents

Sodium hydrogen exchanger inhibitory activity of benzotriazole derivatives

Singh, Dhandeep,Silakari, Om

, p. 183 - 189 (2016/10/25)

Series of benzotriazole derivatives were synthesized and evaluated for their Sodium hydrogen exchanger-1 inhibitory potential. All compounds inhibit Sodium hydrogen exchanger-1 in the in-vitro platelet swelling assay. This is perhaps the first report of NHE-1 inhibitory activity of benzotriazole. The 1-alkyl benzotriazole derivatives were found to be more active than the 2-alkyl isomers. The activity increases with increase in chain length of alkyl moiety. Potency increased from that of benzotriazole (IC50= 192.68 μM) to heptyl derivative (compound 13; IC50= 59.23 μM). Introduction of electronegative oxygen atom further increased potency as shown by the benzoyl (compound 16, IC50= 51.57 μM) and sulfonyl groups (compound 17, IC50= 50.89 μM; compound 18, IC50= 49.95 μM).

Organic reactions in ionic liquids: An efficient method for the N-alkylation of benzotriazole

Le, Zhang-Gao,Chen, Zhen-Chu,Hu, Yi,Zheng, Qin-Guo

, p. 344 - 346 (2007/10/03)

The N-alkylation of benzotriazole with alkyl halides proceeds efficiently in the presence of potassium hydroxide in ionic liquid 1-butyl-3- methylimidazolium tetrafluoroborate ([Bmim][BF4]).

SELECTIVE ALKYLATIONS OF 1,2,4-TRIAZOLE AND BENZOTRIAZOLE IN THE ABSENCE OF SOLVENT

Abenhaim, David,Diez-Barra, Enrique,Hoz, Antonio de la,Loupy, Andre,Sanchez-Migallon, Ana

, p. 793 - 802 (2007/10/02)

Alkylation of 1,2,4-triazole and benzotriazole has been performed either in basic media under solvent free phase transfer catalysis conditions or in the absence of base by conventional and microwave heating.Several parameters affecting the selectivity have been studied.In the case of triazole alkylation, microwave irradiation produces specific (non thermal) effects both on reactivity and selectivity.

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