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4-Cyanophenylglyoxal hydrate, with the molecular formula C9H7NO3, is a hydrate form of 4-cyanophenylglyoxal. It is a yellow to orange solid with a faint odor and is known for its versatile reactivity and functional group compatibility. This chemical compound is a key intermediate in various industrial applications, including the synthesis of pharmaceuticals, agrochemicals, dyes, pigments, and polymers. Its ability to react with amino acids and proteins also makes it significant in the study of biological processes and medicinal chemistry research.

19010-28-7

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19010-28-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Cyanophenylglyoxal hydrate is used as a key intermediate in the synthesis of various pharmaceuticals. Its reactivity and functional group compatibility make it suitable for the development of new drugs and the improvement of existing ones.
Used in Agrochemical Industry:
In the agrochemical industry, 4-cyanophenylglyoxal hydrate is utilized as a crucial component in the production of various agrochemicals. Its role in the synthesis of these compounds contributes to the development of effective solutions for agricultural challenges.
Used in Dye and Pigment Industry:
4-Cyanophenylglyoxal hydrate is employed as a key intermediate in the production of dyes and pigments. Its versatile reactivity allows for the creation of a wide range of colorants used in various applications, such as textiles, plastics, and printing inks.
Used in Polymer Industry:
In the polymer industry, 4-cyanophenylglyoxal hydrate serves as an essential building block for the synthesis of various polymers. Its compatibility with functional groups enables the development of polymers with specific properties, such as improved strength, flexibility, or chemical resistance.
Used in Medicinal Chemistry Research:
4-Cyanophenylglyoxal hydrate is used as a valuable tool in medicinal chemistry research. Its ability to react with amino acids and proteins makes it important for studying biological processes and developing new therapeutic agents.
Overall, 4-cyanophenylglyoxal hydrate plays a crucial role in various industries due to its versatile reactivity and functional group compatibility, making it a valuable compound for the development and production of a wide range of products.

Check Digit Verification of cas no

The CAS Registry Mumber 19010-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,1 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19010-28:
(7*1)+(6*9)+(5*0)+(4*1)+(3*0)+(2*2)+(1*8)=77
77 % 10 = 7
So 19010-28-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H5NO2.H2O/c10-5-7-1-3-8(4-2-7)9(12)6-11;/h1-4,6H;1H2

19010-28-7SDS

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 4-oxaldehydoylbenzonitrile,hydrate

1.2 Other means of identification

Product number -
Other names 4-Cyanophenylglyoxalhydrat

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:19010-28-7 SDS

19010-28-7Downstream Products

19010-28-7Relevant academic research and scientific papers

Synthesis of novel benzamidine- and guanidine-derived polyazamacrocycles: Selective anti-protozoal activity for human African trypanosomiasis

Reid, Caroline M.,Ebikeme, Charles,Barrett, Michael P.,Patzewitz, Eva-Maria,Mueller, Sylke,Robins, David J.,Sutherland, Andrew

, p. 5399 - 5401 (2008)

Efficient synthetic routes have been developed for the preparation of two new polyazamacrocycles tagged with structural motifs recognised by the Trypanosoma brucei P2 aminopurine transporter. Biological testing of these compounds showed highly selective a

A highly efficient and enantioselective intramolecular cannizzaro reaction under TOX/Cu(II) catalysis

Wang, Pan,Tao, Wen-Jie,Sun, Xiu-Li,Liao, Saihu,Tang, Yong

supporting information, p. 16849 - 16852 (2013/12/04)

An asymmetric intramolecular Cannizzaro reaction of aryl and alkyl glyoxals with alcohols has been realized with an unprecedented high level of enantioselectivity, on the basis of a newly developed congested TOX ligand and a gradual liberation protocol of active glyoxals from glyoxal monohydrates. Preliminary results suggested a mechanism of enantioselective addition of alcohols to glyoxals contributing most to the stereoselectivity, other than by the dynamic kinetic resolution of hemiacetal intermediates.

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