106429-67-8

Basic information

• Product Name: (1H-BENZO[D][1,2,3]TRIAZOL-5-YL)METHANOL
• Synonyms: (1H-BENZO[D][1,2,3]TRIAZOL-5-YL)METHANOL
• CAS NO: 106429-67-8
• Molecular Formula: C₇H₇N₃O
• Molecular Weight: 149.14998
• Mol File: 106429-67-8.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 388.9°C at 760 mmHg
• Flash Point: 189°C
• Appearance: /
• Density: 1.46g/cm³
• Vapor Pressure: 9.62E-07mmHg at 25°C
• Refractive Index: 1.739
• PKA: 8.38±0.40(Predicted)
• CAS DataBase Reference: (1H-BENZO[D][1,2,3]TRIAZOL-5-YL)METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (1H-BENZO[D][1,2,3]TRIAZOL-5-YL)METHANOL(106429-67-8)
• EPA Substance Registry System: (1H-BENZO[D][1,2,3]TRIAZOL-5-YL)METHANOL(106429-67-8)

Safety Data

• Hazardous Substances Data: 106429-67-8(Hazardous Substances Data)

Usage

General Description

(1H-Benzo[d][1,2,3]triazol-5-yl)methanol is a chemical compound with the molecular formula C8H7N3O. It is a benzotriazole compound, which is commonly used as a corrosion inhibitor for metals, particularly in the aerospace and automotive industries. It is also used as an intermediate in the synthesis of pharmaceuticals, dyes, and other organic compounds. The compound has a triazole ring structure, which makes it suitable for various applications in organic chemistry, including as a stabilizer for polymers and UV-absorber in plastics. Additionally, it has been studied for its potential anti-inflammatory and anti-cancer properties, making it a versatile and valuable compound in various industries.

InChI:InChI=1/C7H7N3O/c11-4-5-1-2-6-7(3-5)9-10-8-6/h1-3,11H,4H2,(H,8,9,10)

Upstream product

• 491612-10-3 C₈H₇N₃O₂ 
• 1246639-99-5 C₁₀H₁₁N₃O₂ 
• 442911-05-9 tert-butyl 5-methylbenzotriazole-1-carboxylate 
• 136-85-6 5⁽⁶⁾-methylbenzotriazole 
• 23814-12-2 1h-benzotriazole-5-carboxylic acid 
• 113053-50-2 1H-Benzotriazole-5-carboxylic acid methyl ester 
• 73605-91-1 1H-benzotriazole-5-carboxylic acid ethyl ester 

Downstream Products

• 70938-42-0 1H-1,2,3-benzotriazole-5-carbaldehyde 

Relevant articles and documents

Synthesis of 5,5-di-(benzotriazol-5-ylmethyl)-2,2-dimethyl-1,3-dioxane-4,6-dione and 5-(benzotriazol-5-ylmethyl)-2,2,5-trimethyl-1,3-dioxane-4.6-dione

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Passivation solution Treated copper foil and lithium battery packaging film comprising same

The invention relates to a methyl benzotriazole derivative passivator, passivating liquid containing the passivator, a copper foil treated by the passivating liquid, and a lithium battery packaging film containing the copper foil. The structure of a methyl benzotriazole derivative is shown in a formula (I). The copper foil passivated by treatment liquid containing the passivator has strong adhesive force with a polyolefin adhesive and a polyurethane adhesive, and when the copper foil is applied to the lithium battery packaging film, and the obtained lithium battery packaging film is stable instructure and has long service life, excellent stamping performance and electrolyte resistance.

Substituted Pyran Derivatives

Certain 3,6-disubstituted and 2, 4, 5-trisubstituted pyran derivatives that exhibit potent activity on monoamine transport systems are provided. The 3, 6 and 2, 4, 5 pyrans are useful in probing the effects of their binding to monoamine transporter system

NOVEL CURCUMIN DERIVATIVE

The present invention provides a novel compound that is structurally similar to curcumin and has a suppressive effect on Aβ aggregation, a degradative effect on Aβ aggregates, an inhibitory effect on β-secretase, and a protective effect on neurons. The novel compound is a compound represented by the following general formula (Ia) or a salt thereof: wherein R1 represents a 4-hydroxy-3-methoxyphenyl group or the like, and R2 represents a 1H-indol-6-yl group or the like.