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Hydrocarboxyl radicals are a class of organic compounds that contain a hydrocarboxyl group, which is a combination of a hydroxyl (-OH) and a carboxyl (-COOH) functional group. These radicals are characterized by the presence of a carbon-carbon double bond (C=C) adjacent to the hydrocarboxyl group, forming an α,β-unsaturated carboxylic acid structure. They play a significant role in various chemical reactions, such as polymerization, esterification, and oxidation, and are found in natural products like terpenes and fatty acids. Hydrocarboxyl radicals are also involved in the biosynthesis of essential compounds in living organisms, making them an important area of study in organic chemistry and biochemistry.

2564-86-5

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2564-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2564-86-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2564-86:
(6*2)+(5*5)+(4*6)+(3*4)+(2*8)+(1*6)=95
95 % 10 = 5
So 2564-86-5 is a valid CAS Registry Number.
InChI:InChI=1/CHO2/c2-1-3/h1H

2564-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name hydroxidooxidocarbon(?)

1.2 Other means of identification

Product number -
Other names Carboxyl-radikal

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:2564-86-5 SDS

2564-86-5Downstream Products

2564-86-5Relevant academic research and scientific papers

Formation of Glyoxylic Acid in Interstellar Ices: A Key Entry Point for Prebiotic Chemistry

Eckhardt, André K.,Bergantini, Alexandre,Singh, Santosh K.,Schreiner, Peter R.,Kaiser, Ralf I.

supporting information, p. 5663 - 5667 (2019/03/29)

With nearly 200 molecules detected in interstellar and circumstellar environments, the identification of the biologically relevant α-keto carboxylic acid, glyoxylic acid (HCOCOOH), is still elusive. Herein, the formation of glyoxylic acid via cosmic-ray driven, non-equilibrium chemistry in polar interstellar ices of carbon monoxide (CO) and water (H2O) at 5 K via barrierless recombination of formyl (HCO) and hydroxycarbonyl radicals (HOCO) is reported. In temperature-programmed desorption experiments, the subliming neutral molecules were selectively photoionized and identified based on the ionization energy and distinct mass-to-charge ratios in combination with isotopically labeled experiments exploiting reflectron time-of-flight mass spectrometry. These studies unravel a key reaction path to glyoxylic acid, an organic molecule formed in interstellar ices before subliming in star-forming regions like SgrB2(N), thus providing a critical entry point to prebiotic organic synthesis.

Products of the ultraviolet photodissociation of trifluoroacetic acid and acrylic acid

Osborne, Michael C.,Li, Qiang,Smith, Ian W. M.

, p. 1447 - 1454 (2007/10/03)

The photodissociation of trifluoroacetic and acrylic acids by the ultraviolet light from a flashlamp has been investigated by measuring the relative yields of some of the major products by time-resolved infrared absorption using tunable, narrow band diode lasers. Yields of CO2 were measured both in the absence and presence of added O2. The former experiments measure the CO2 produced directly by decarboxylation of the acid, channel (2) below, the latter the sum of the yields from channels (1) and (2) since HOCO is rapidly converted to CO2. The yields of CO from the decarbonylation channel (3) have also been measured. For trifluoroacetic acid, the relative yields are found to be [HOCO]: [CO2]: [CO] = (0.28 ± 0.07): (0.61 ± 0.09): (0.11 ± 0.06) and, for acrylic acid, [HOCO]: [CO2]: [CO] = (0.32 ± 0.08): (0.37 ± 0.08) :(0.31 ± 0.09). The results are discussed in relation to the other, limited, measurements on the photodissociation of these acids and whether these three processes are likely to occur independently of one another.

Experimental Study and Kinetic Modeling of Propene Oxidation in a Jet Stirred Flow Reactor

Dagaut, P.,Cathonnet, M.,Boettner J. C.

, p. 661 - 671 (2007/10/02)

The oxidation of propene was studied in a jet stirred flow reactor in the temperature range 900-1200 K at pressures extending from 1 to 8 atm for a wide range of fuel-oxygen equivalence ratios (0.15-4.0).A computer program has been developed to model the experimental data by using a chemical kinetic reaction mechanism.A direct method to determine the first-order sensitivities of the mole fraction of each species with respect to the rate constants was used to develop the kinetic scheme.The present chemical kinetic reaction mechanism is able to reproduce the experimental results, although some discrepancies are observed for the minor products.

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