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di(prop-2-yn-1-yl) oxalate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71573-77-8

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71573-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71573-77-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,7 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71573-77:
(7*7)+(6*1)+(5*5)+(4*7)+(3*3)+(2*7)+(1*7)=138
138 % 10 = 8
So 71573-77-8 is a valid CAS Registry Number.

71573-77-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(prop-2-ynyl) oxalate

1.2 Other means of identification

Product number -
Other names Ethanedioic acid,di-2-propynyl ester

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:71573-77-8 SDS

71573-77-8Downstream Products

71573-77-8Relevant academic research and scientific papers

The rate coefficient of the C3H3 + C 3H3 reaction from UV absorption measurements after photolysis of dipropargyl oxalate

Giri,Hippler,Olzmann,Unterreiner

, p. 4641 - 4646 (2003)

The kinetics of the C3H3 + C3H 3 reaction was investigated by using dipropargyl oxalate (DPO) as a new, halogen-free photolytic source for propargyl radicals in the gas phase. After laser-flash photolysis of DPO at 193 nm, the initial absorbance was determined at different wavelengths, and the results were compared with values obtained in analogous experiments using propargyl halides as precursors. A satisfactory agreement of the absorbances was found between 295 and 355 nm but differences were observed near 242 nm. The latter wavelength has also been proposed for C3H3 detection. Our results, however, indicate that this absorption is probably due to halogen-containing species. The rate coefficient of the C3H3 + C3H 3 reaction was then determined from time-resolved absorption measurements at 332.5 nm with DPO as precursor. Values of (2.7 ± 0.6) × 10-11 cm3 molecule-1 s-1 at 373 K, (2.8 ± 0.6) × 10-11 cm3 molecule -1 s-1 at 425 K, (3.5 ± 0.8) × 10 -11 cm3 molecule-1 s-1 at 500 K, and (4.1 ± 0.8) × 10-11 cm3 molecule -1 s-1 at 520 K were obtained with no significant pressure dependence between 1 and ca. 100 bar (140 bar for T = 373 K).

Novel syntheses of oxamides, oxamates and oxalates from diisopropenyl oxalate

Neveux, Muriel,Bruneau, Christian,Lecolier, Serge,Dixneuf, Pierre H.

, p. 2629 - 2640 (2007/10/02)

Diisopropenyl oxalate, obtained by catalytic addition of oxalic acid to propyne, is a useful reagent for the access to a variety of α-dicarbonyl compounds such as oxamides, oxamates and oxalates, under very mild conditions.

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