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2-keto-3-butynoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56842-75-2

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56842-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56842-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,4 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56842-75:
(7*5)+(6*6)+(5*8)+(4*4)+(3*2)+(2*7)+(1*5)=152
152 % 10 = 2
So 56842-75-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H2O3/c1-2-3(5)4(6)7/h1H,(H,6,7)

56842-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxobut-3-ynoic acid

1.2 Other means of identification

Product number -
Other names 2-Oxo-3-butynoate

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:56842-75-2 SDS

56842-75-2Upstream product

56842-75-2Downstream Products

56842-75-2Relevant academic research and scientific papers

Ethynylhydroxycarbene (H-CC-C¨-OH)

Bernhardt, Bastian,Ruth, Marcel,Eckhardt, André K.,Schreiner, Peter R.

, p. 3741 - 3746 (2021)

The species on the C3H2O potential energy surface have long been known to play a vital role in extraterrestrial chemistry. Here we report on the hitherto uncharacterized isomer ethynylhydroxycarbene (H-CC-C¨-OH, 1) generated by high-vacuum flash pyrolysis of ethynylglyoxylic acid ethyl ester and trapped in solid argon matrices at 3 and 20 K. Upon irradiation at 436 nm trans-1 rearranges to its higher lying cis-conformer. Prolonged irradiation leads to the formation of propynal. When the matrix is kept in the dark, 1 reacts within a half-life of ca. 70 h to propynal in a conformer-specific [1,2]H-tunneling process. Our results are fully consistent with computations at the CCSD(T)/cc-pVTZ and the B3LYP/def2-QZVPP levels of theory.

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