115-17-3

Basic information

• Product Name: Tribromoacetaldehyde
• Synonyms: TRIBROMOACETALDEHYDE;TRIBROMOACETYLALDEHYDE;2,2,2-Tribromoacetaldehyde;tribromo-acetaldehyd;Tribromoethanal;BROMAL;BROMAL, REDIST.;Tribromo
• CAS NO: 115-17-3
• Molecular Formula: C₂HBr₃O
• Molecular Weight: 280.74
• EINECS: 204-067-9
• Mol File: 115-17-3.mol
• Article Data: 6

Chemical Properties

• Melting Point: -57.5 °C
• Boiling Point: 174 °C(lit.)
• Flash Point: 150 °F
• Appearance: /
• Density: 2.665 g/mL at 25 °C(lit.)
• Vapor Pressure: 1.23mmHg at 25°C
• Refractive Index: n20/D 1.584(lit.)
• Storage Temp.: Refrigerator (+4°C)
• Water Solubility: Soluble in water
• Merck: 14,1383
• BRN: 1098614
• CAS DataBase Reference: Tribromoacetaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: Tribromoacetaldehyde(115-17-3)
• EPA Substance Registry System: Tribromoacetaldehyde(115-17-3)

Safety Data

• Hazard Codes: T+,Xi,T
• Statements: 25-27-34
• Safety Statements: 26-28-36/37/39-45-28A
• RIDADR: UN 2927 6.1/PG 1
• WGK Germany: 3
• RTECS: AB3237500
• F: 3-8-10-19
• HazardClass: 8
• PackingGroup: III
• Hazardous Substances Data: 115-17-3(Hazardous Substances Data)

Usage

Description

Tribromoacetaldehyde is an organic compound with the chemical formula C2HBr3O2. It is an oily, yellowish liquid that is soluble in water, alcohol, or ether. Tribromoacetaldehyde is known for its combustible properties, making it a versatile compound in various applications.

Uses

Used in Organic Synthesis:
Tribromoacetaldehyde is used as an intermediate in the synthesis of various organic compounds. Its unique chemical properties, including its solubility and combustibility, make it a valuable component in the creation of different chemical products.
Used in Chemical Industry:
In the chemical industry, Tribromoacetaldehyde is utilized as a building block for the production of a range of chemicals. Its reactivity and solubility in common solvents facilitate its use in various chemical reactions, contributing to the development of new materials and compounds.
Used in Pharmaceutical Industry:
Tribromoacetaldehyde may also find applications in the pharmaceutical industry, where it can be used as a starting material for the synthesis of pharmaceutical compounds. Its properties can be harnessed to create new drugs or improve the synthesis process of existing ones.
Used in Research and Development:
Due to its unique chemical characteristics, Tribromoacetaldehyde is also used in research and development settings. Scientists and researchers can explore its properties and reactivity to discover new applications and improve existing processes in various fields, including materials science and biotechnology.

Upstream product

• 105-57-7 diethyl acetal 
• 60-29-7 diethyl ether 
• 64-17-5 ethanol 
• 33243-81-1 2,2,2-tribromo-1-ethoxy-ethanol 
• 75-87-6 chloral 
• 123-63-7 paracetaldehyde 
• 507-42-6 bromal hydrate 
• 135728-18-6 2,2,2-tris-(2,2,2-tribromo-1-chloroethoxy)-1,3,2λ⁵-benzodioxaphosphole 
• 499-50-3 uvitonic acid 
• 7732-18-5 water 
• 7726-95-6 bromine 
• 141-78-6 ethyl acetate 
• 107-07-3 2-chloro-ethanol 
• 105-58-8 Diethyl carbonate 

Downstream Products

• 567-54-4 1,1,1-tribromo-2,2-bis-(4-fluoro-phenyl)-ethane 
• 500790-39-6 1,1,1-tribromo-2,2-bis-(4-bromo-phenyl)-ethane 
• 102305-56-6 phosphoric acid-(2,2-dibromo-vinyl ester)-diisopropyl ester 
• 105207-74-7 2-phenyl-butyric acid-(2,2,2-tribromo-1-hydroxy-ethylamide) 
• 75-80-9 2,2,2-tribromoethanol 
• 58577-58-5 1,1,1-tribromo-butan-2-ol 
• 75-25-2 Bromoform 
• 2909-52-6 tribromo(2H)methane 
• 507-42-6 bromal hydrate 
• 75-96-7 tribromoacetic acid 
• 88837-72-3 2,2-bis(4-methoxyphenyl)-1,1,1-tribromoethane 

Related news

On the blue-shifting hydrogen bond in Tribromoacetaldehyde (cas 115-17-3) dimers08/22/2019

The dimerisation of tribromoacetaldehyde in CCl4 and C6D12 solutions was investigated using Raman spectroscopy and different techniques of multivariate analysis. The ν(C–H) stretching vibration band in dimers was blue shifted by 14/15 cm−1, whereas the ν(CO) dimer band was red-shifted by 7/8 ...detailed

Relevant articles and documents

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Para-hydroxyalkylation of hydroxylated aromatic compounds

Hydroxylated aromatic compounds devoid of substituents in the para-position to the hydroxyl group thereof are para-hydroxyalkylated, e.g., into optionally substituted p-hydroxymandelic acid compounds, more particularly p-hydroxymandelic acid and 3-methoxy-p-hydroxymandelic acid, by condensing same with an organic carbonyl compound in the presence of a quaternary ammonium hydroxide.

INVESTIGATION OF THE BEHAVIOR OF POLYHALOGENATED ALDEHYDE HYDRATES IN SOLUTIONS BY THE PMR METHOD

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