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5883-81-8

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5883-81-8 Usage

Physical State

Pale yellow solid

Common Uses

Intermediate in pharmaceutical synthesis
Intermediate in dye synthesis
Intermediate in organic compound synthesis
Building block in organic chemistry
Catalyst in chemical reactions
Precursor in fragrance and flavoring production

Chemical Functionality

Aromatic ketone (acetophenone)
Aniline (phenylamine)

Versatility

Used in preparation of heterocyclic compounds
Used in preparation of complex molecules

Toxicity

Considered of moderate toxicity

Safety Precautions

Proper handling required
Adherence to safety protocols necessary

Check Digit Verification of cas no

The CAS Registry Mumber 5883-81-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,8 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5883-81:
(6*5)+(5*8)+(4*8)+(3*3)+(2*8)+(1*1)=128
128 % 10 = 8
So 5883-81-8 is a valid CAS Registry Number.

5883-81-8Relevant articles and documents

Visible-Light-Induced Oxidative α-Alkylation of Glycine Derivatives with Ethers under Metal-Free Conditions

Song, Yang,Zhang, Hao,Guo, Jiabao,Shao, Yifei,Ding, Yuzhou,Zhu, Li,Yao, Xiaoquan

, p. 5914 - 5921 (2021/11/22)

In this work, a visible-light-induced oxidative α-alkylation of glycine derivatives with ethers has been developed in the presence of catalytic Eosin Y. Under the blue light of a 3 W LED, a range of α-etherized glycine derivatives, including α-amino esters, α-amino ketones and α-amino amides, were achieved with good to excellent yields and functional group tolerance with tert-butyl hydroperoxide (TBHP) as oxidant at ambient temperature. The operationally easy procedure provides an economical, metal-free, and mild alternative for the synthesis of the α-etherized glycine derivatives.

Design and discovery of new antiproliferative 1,2,4-triazin-3(2H)-ones as tubulin polymerization inhibitors targeting colchicine binding site

Eissa, Ibrahim H.,Dahab, Mohammed A.,Ibrahim, Mohamed K.,Alsaif, Nawaf A.,Alanazi,Eissa, Sally I.,Mehany, Ahmed B.M.,Beauchemin, André M.

, (2021/05/26)

Thirty-five new colchicine binding site inhibitors have been designed and synthesized based on the 1,2,4-triazin-3(2H)-one nucleus. Such molecules were synthesized through a cascade reaction between readily accessible α-amino ketones and phenyl carbazate

Regioselective Synthesis of 2-Arylindoles via Palladium-Catalyzed Cyclization of Phenylglyoxal and 2-Anilinoacetophenones with Anilines

Benitez-Medina, G. Eliad,Ortiz-Soto, Sofía,Cabrera, Armando,Amézquita-Valencia, Manuel

, p. 3763 - 3770 (2019/06/24)

A versatile route has been developed for the synthesis of 2-arylindoles using a Pd-catalyzed tandem process. Under reductive conditions, different 2-arylindoles were synthesized from phenylglyoxal and aniline. This synthetic methodology involves a tandem reaction of four steps with high regioselectivity. Alternatively, 2-anilinoacetophenones intermediates also can be using to give access to the corresponding 2-arylindoles.

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