131922-15-1 Usage
General Description
2-Benzofuranyl glyoxal hydrate is a chemical compound commonly used in the synthesis of organic compounds and pharmaceuticals. It is a versatile building block that can be used to create a variety of different types of molecules, including those with medicinal applications. The compound is known for its reactivity with various functional groups, allowing for the formation of complex structures. Additionally, 2-Benzofuranyl glyoxal hydrate is known for its ability to act as a catalyst in certain chemical reactions, further enhancing its potential uses in organic synthesis. Overall, it is an important tool for chemists and pharmaceutical researchers in the development of new drugs and organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 131922-15-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,9,2 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 131922-15:
(8*1)+(7*3)+(6*1)+(5*9)+(4*2)+(3*2)+(2*1)+(1*5)=101
101 % 10 = 1
So 131922-15-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H6O3.H2O/c11-6-8(12)10-5-7-3-1-2-4-9(7)13-10;/h1-6H;1H2
131922-15-1Relevant articles and documents
Metal-free dual sp3 C-H functionalization: I2- promoted domino oxidative cyclization to construct 2,5-disubstituted oxazoles
Gao, Qing-He,Fei, Zhuan,Zhu, Yan-Ping,Lian, Mi,Jia, Feng-Cheng,Liu, Mei-Cai,She, Neng-Fang,Wu, An-Xin
, p. 22 - 28 (2013/01/15)
An I2-promoted sp3 C-H functionalization has been developed for the synthesis of 2,5-disubstituted oxazoles from easily available methyl ketones and benzylamines without any metal and peroxide catalyst. This domino oxidative cyclization process involves the cleavage of C-H bond and the formation of C-N, C-O bonds.
Reactions of α-imino ketones derived from arylglyoxals with (trifluoromethyl)trimethylsilane; A new route to β-amino-α- trifluoromethyl alcohols
Mloston, Grzegorz,Obijalska, Emilia,Tafelska-Kaczmarek, Agnieszka,Zaidlewicz, Marek
scheme or table, p. 1289 - 1296 (2011/02/22)
The reactions of α-imino ketones, derived from arylglyoxals, with (trifluoromethyl)trimethylsilane (CF3SiMe3) in DME solution, in the presence of catalytic amount of CsF, at room temperature, yield O-silylated β-imino alcohols in the
