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Phenyl-vinyl-glykolsaeure, also known as phenyl vinyl glycolic acid, is a chemical compound with the molecular formula C8H8O3. It is a derivative of glycolic acid, featuring a phenyl group and a vinyl group attached to the hydroxyl-bearing carbon atom. This organic acid is characterized by its unique structure, which combines the properties of both phenyl and vinyl groups, making it a versatile building block in organic synthesis. Phenyl-vinyl-glykolsaeure is used in the production of various pharmaceuticals, agrochemicals, and specialty chemicals, owing to its reactivity and ability to form esters, amides, and other functional groups. Its applications span across different industries, highlighting its importance in chemical research and development.

1626-05-7

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1626-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1626-05-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1626-05:
(6*1)+(5*6)+(4*2)+(3*6)+(2*0)+(1*5)=67
67 % 10 = 7
So 1626-05-7 is a valid CAS Registry Number.

1626-05-7Relevant academic research and scientific papers

Domino Synthesis of α,β-Unsaturated γ-Lactams by Stereoselective Amination of α-Tertiary Allylic Alcohols

Xie, Jianing,Xue, Sijing,Escudero-Adán, Eduardo C.,Kleij, Arjan W.

, p. 16727 - 16731 (2018)

Tertiary allylic alcohols equipped with a carboxyl group can be smoothly aminated under ambient conditions by a conceptually new and stereoselective protocol under palladium catalysis. The in situ formed Z-configured γ-amino acid cyclizes to afford an α,β-unsaturated γ-lactam, releasing water as the only byproduct. This practical catalytic transformation highlights the use of a carboxyl group acting as an activating and stereodirecting functional group to provide a wide series of pharma-relevant building blocks. Various control reactions support the crucial role of the carboxyl group in the substrate to mediate these transformations.

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