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(2-Formamido-1,3-thiazol-4-yl)glyoxylic acid is a chemical compound that belongs to the class of organic compounds known as thiazoles. These are heterocyclic compounds characterized by a ring structure that includes a sulfur atom and a nitrogen atom. This particular compound is distinguished by the presence of a 2-formamido-1,3-thiazol-4-yl functional group and a glyoxylic acid group. Although its specific properties, such as reactivity, stability, and applications, are not extensively documented, it is likely used in specialized research or industrial applications. Given its structural features, it may have potential uses in synthetic chemistry, pharmaceuticals, or materials science.

64987-06-0

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64987-06-0 Usage

Uses

Used in Synthetic Chemistry:
(2-Formamido-1,3-thiazol-4-yl)glyoxylic acid is used as a building block or intermediate in the synthesis of more complex molecules, particularly in the field of organic chemistry. Its unique functional groups can be exploited to form a variety of chemical bonds, making it a valuable component in the creation of novel compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2-Formamido-1,3-thiazol-4-yl)glyoxylic acid may serve as a key component in the development of new drugs. Its structure could potentially be incorporated into drug molecules to enhance their therapeutic effects or to improve their pharmacokinetic properties, such as absorption, distribution, metabolism, and excretion.
Used in Materials Science:
(2-Formamido-1,3-thiazol-4-yl)glyoxylic acid could be utilized in the development of new materials with specific properties, such as improved stability or reactivity. Its incorporation into material compositions may lead to advancements in areas like polymer science, where it could contribute to the creation of materials with tailored characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 64987-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,8 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64987-06:
(7*6)+(6*4)+(5*9)+(4*8)+(3*7)+(2*0)+(1*6)=170
170 % 10 = 0
So 64987-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H4N2O4S/c9-2-7-6-8-3(1-13-6)4(10)5(11)12/h1-2H,(H,11,12)(H,7,8,9)

64987-06-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-Formamido-1,3-thiazol-4-yl)glyoxylic acid

1.2 Other means of identification

Product number -
Other names 2-formylaminothiazol-4-ylglyoxylic acid

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:64987-06-0 SDS

64987-06-0Relevant articles and documents

Synthesis and Pharmacological Evaluation of a New Class of 2-(2-Aminothiazol-4-yl)-2-hydrazonoacetamido Cephalosporins

Brandt, Alberto,Cerquetti, Marina,Corsi, G. Bruno,Pascucci, Giorgio,Simeoni, Antonio,et al.

, p. 764 - 767 (2007/10/02)

A series of 2-(2-aminothiazol-4-yl)-2-hydrazonoacetamido cephalosporins 1a-h was prepared.Whenever possible, E and Z isomers were isolated, and their relative stabilities and their interconversions were tested.The antibacterial activity was tested against Gram-positive and Gram-negative bacteria.For compound 1c, whose Z and E forms do not interconvert rapidly, the Z form was the more active one.Among the other compounds, for which the E form is the only stable one for practical purposes, compound 1a was the most active.When compared with cefuroxime and cefotaxime, compound 1a showed slightly lower antibacterial activity but good serum level and half-life values.

Process for producing 2-(2-aminothiazol-4-yl)glyoxylic acid derivative or a salt thereof, and intermediates therefor and process for producing the intermediates

-

, (2008/06/13)

This invention relates to a novel process for producing a 2-(2-aminothiazol-4-yl)glyoxylic acid derivative or a salt thereof which are useful in producing a cephalosporin antibiotic, and to intermediates for said derivative and salt and a process for producing the intermediates.

2-Lower alkyl-7-substituted-2 or 3-cephem 4-carboxylic acid compounds

-

, (2008/06/13)

Compounds of the formula: STR1 wherein R1 is (C1 to C6) alkyl. R2 is carboxy or a protected carboxy group, R3 is amino or a protected amino group and A is hydroxyimino (C1 to C6) alkylene or (C1 to C6)-alkoxyimino (C1 to C6) alkylene, and pharmaceutically acceptable salt thereof, have been found to be active against various pathogenic microorganisms.

2-Lower alkyl-7-substituted amino-2 or 3-cephem-4-carboxylic acid compounds

-

, (2008/06/13)

A compound of the formula: STR1 wherein R1 is (C1 to C6) alkyl, R2 is carboxy or a protected carboxy group, R3 is amino or a protected amino group, and A is carbonyl or hydroxy (C1 to C6) alkylene, and pharmaceutically acceptable salt thereof, which is active against pathogenic bacteria, and methods for preparing the same.

2-Lower alkyl-7-substituted-2 or 3-cephem-4-carboxylic acid compounds and pharmaceutical compositions

-

, (2008/06/13)

A compound of the formula: STR1 wherein R1 is (C1 to C6) alkyl, R2 is a carboxy or a protected carboxy group, R3 is amino or a protected amino group and A is hydroxyimino (C1 to C6) alkylene or (C1 to C6)-alkoxyimino (C1 to C6)alkylene, And pharmaceutically acceptable salt thereof.

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