92283-88-0

Basic information

• Product Name: Benzotriazole1.0
• Synonyms: 1.5;Benzotriazole1.0;2,3-Dianhydro-4,6-O-benzylidene-D-allitol;1,5:2,3-dianhydro-4,6-O-[(R)-phenylMethylene]-D-Allitol;(1aS,3aR,6R,7aR,7bS)-6-Phenylhexahydrooxireno[2',3':4,5]pyrano[3,2-d][1,3]dioxine
• CAS NO: 92283-88-0
• Molecular Formula: C₁₃H₁₄O₄
• Molecular Weight: 234.24786
• Mol File: 92283-88-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzotriazole1.0(CAS DataBase Reference)
• NIST Chemistry Reference: Benzotriazole1.0(92283-88-0)
• EPA Substance Registry System: Benzotriazole1.0(92283-88-0)

Safety Data

• Hazardous Substances Data: 92283-88-0(Hazardous Substances Data)

Usage

General Description

Benzotriazole 1.0 is a chemical compound that is commonly used as a corrosion inhibitor in industrial applications, especially in metalworking and metal cleaning processes. It is known for its ability to effectively protect metals from corrosion and oxidation by forming a thin and stable protective layer on the metal surface. Additionally, benzotriazole 1.0 is also used as a stabilizer in the production of plastics, adhesives, and coatings to prevent degradation due to exposure to UV radiation. This versatile chemical is considered to be environmentally friendly and is widely used in various industries to improve the durability and longevity of metal and plastic products.

Upstream product

• 65391-44-8 1,5-anhydro-4,6-O-(R)-benzylidene-D-glucitol 
• 65371-07-5 2,3-di-O-p-tolylsulphonyl-4,6-O-benzylidene-1,5-anhydro-D-glucitol 

Downstream Products

• 1117903-22-6 1,5-anhydro-4-O-(tert-butyldimethylsilyl)-2,3-dideoxy-6-O-(4,4'-dimethoxytrityl)-3-fluoro-2-(thymin-1-yl)-D-altritol 
• 1117903-17-9 1,5-anhydro-4,6-O-benzylidene-2-deoxy-3-O-methanesulfonyl-2-(thymin-1-yl)-D-altritol 
• 1117903-18-0 1,5-anhydro-4,6-O-benzylidene-2-deoxy-2-(thymin-1-yl)-D-mannitol 
• 1117903-19-1 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-fluoro-2-(thymin-1-yl)-D-altritol 
• 1117903-20-4 1,5-anhydro-2,3-dideoxy-6-O-(4,4'-dimethoxytrityl)-3-fluoro-2-(thymin-1-yl)-D-altritol 
• 1117903-21-5 1,5-anhydro-4-O-(2-cyanoethoxydiisopropylaminophosphinyl)-2,3-dideoxy-6-O-(4,4'-dimethoxytrityl)-3-fluoro-2-(thymin-1-yl)-D-altritol 
• 92237-27-9 2-deoxy-2-bromo-4,6-O-benzylidene-1,5-anhydro-D-altritol 
• 84109-66-0 (2R,4R,5S)-2-phenyl-4-<(1S)-1-hydroxyprop-2-enyl>-5-hydroxy-1,3-dioxane 
• 92237-25-7 2-deoxy-2-C-allyl-4,6-O-benzylidene-1,5-anhydro-D-altritol 
• 92237-23-5 2-deoxy-2-C-vinyl-4,6-O-benzylidene-1,5-anhydro-D-altritol 
• 92237-23-5 2-deoxy-2-C-vinyl-4,6-O-benzylidene-1,5-anhydro-D-allitol 
• 92237-22-4 2-deoxy-2-C-methyl-4,6-O-benzylidene-1,5-anhydro-D-altritol 
• 65190-39-8 O⁴,O⁶-((R)-benzyliden)-1,5-anhydro-D-altritol 

Relevant articles and documents

Unusual Stereochemistry in the Copper-catalyses Ring Opening of a Carbohydrate Oxirane with Vinylmagnesium Bromide

The oxirane ring of 4,6-O-benzylidene-1,5:2,3-dianhydro-D-allitol (1) opened regio- and stereo-selectively at C-2 with Me2CuLi and allylmagnesium chloride in the presence of catalytic amounts of CuI.With vinylmagnesium bromide, however, the ring opening of (1) was regioselective but a mixture of stereoisomers (10) and (12) was obtained corresponding to retention and inversion at C-2.A mechanism for the formation of the anomalous retention product (12) is proposed.