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Ethyl N-benzyl-N-(prop-2-yn-1-yl)carbamate is a chemical compound with the molecular formula C14H17NO2. It is an organic compound that belongs to the class of carbamates, which are derivatives of carbamic acid. This specific compound features a benzyl group (C6H5CH2-) and a prop-2-yn-1-yl group (HC≡CCH2-) attached to the nitrogen atom of the carbamate moiety. The ethyl group (C2H5-) is connected to the oxygen atom. Ethyl N-benzyl-N-(prop-2-yn-1-yl)carbamate is a colorless liquid with a molecular weight of 229.29 g/mol. It is used in various chemical reactions and as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Due to its reactivity, it is important to handle ethyl N-benzyl-N-(prop-2-yn-1-yl)carbamate with care, following proper safety protocols.

2532-71-0

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2532-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2532-71-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,3 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2532-71:
(6*2)+(5*5)+(4*3)+(3*2)+(2*7)+(1*1)=70
70 % 10 = 0
So 2532-71-0 is a valid CAS Registry Number.

2532-71-0Relevant academic research and scientific papers

α-Hydroxy-Tetrazoles as Latent Ethynyl Moieties: A Mechanistic Investigation

Quinodoz, Pierre,Wright, Karen,Drouillat, Bruno,Kletskii, Mikhail E.,Burov, Oleg N.,Lisovin, Anton. V.,Couty, Fran?ois

, (2018/05/03)

This article focuses on the dehydration of α-hydroxy-tetrazoles, leading to tetraazafulvenes and then to vinylic carbenes that rearrange into ethynyl moieties through the Fritsch-Buttenberg-Wiechell rearrangement. Each step of this sequence was scrutinized, either by examination of the substrate and/or dehydrating agent scope, or through AM1 calculations, in order to understand the limiting step of this process. This underrated transformation appears to be a viable alternative to existing methods used for transforming aldehydes into alkynes.

SYNTHESIS OF 5-ALKYNYLIDENE-OXAZOLIDIN-2-ONES

Tam, Tim F.,Thomas, Everton,Krantz, Allen

, p. 1127 - 1130 (2007/10/02)

N-Carboethoxy-N-alkyl-propargylamines react with iodine, silver tetrafluoroborate and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride to give N-alkyl-5(E)-iodomethylidene-oxazolidin-2-ones which can be converted to the corresponding 5-alkynyli

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