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118994-84-6

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118994-84-6 Usage

General Description

Oxazole-4-carbaldehyde is a chemical compound that belongs to the oxazole family, which is a five-membered heterocyclic ring containing one oxygen and one nitrogen atom. This specific compound is an aldehyde, meaning it has a functional group consisting of a carbon atom double-bonded to an oxygen atom and single-bonded to a hydrogen atom. Oxazole-4-carbaldehyde is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and dyes due to its versatile reactivity and ability to participate in a wide range of chemical reactions. It has also been studied for its potential as a precursor in the development of new organic materials and optoelectronic devices. Furthermore, oxazole-4-carbaldehyde has shown promise in the field of medicinal chemistry, where it exhibits biological activities such as antimicrobial and antioxidant properties, making it a versatile and valuable chemical compound in various industrial and scientific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 118994-84-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,9,9 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 118994-84:
(8*1)+(7*1)+(6*8)+(5*9)+(4*9)+(3*4)+(2*8)+(1*4)=176
176 % 10 = 6
So 118994-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H3NO2/c6-1-4-2-7-3-5-4/h1-3H

118994-84-6 Well-known Company Product Price

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  • TCI America

  • (O0453)  4-Oxazolecarboxaldehyde  >98.0%(GC)

  • 118994-84-6

  • 200mg

  • 990.00CNY

  • Detail
  • TCI America

  • (O0453)  4-Oxazolecarboxaldehyde  >98.0%(GC)

  • 118994-84-6

  • 1g

  • 3,450.00CNY

  • Detail
  • Aldrich

  • (697915)  4-Oxazolecarboxaldehyde  97%

  • 118994-84-6

  • 697915-250MG

  • 1,143.09CNY

  • Detail
  • Aldrich

  • (697915)  4-Oxazolecarboxaldehyde  97%

  • 118994-84-6

  • 697915-1G

  • 2,896.92CNY

  • Detail

118994-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Oxazolecarboxaldehyde

1.2 Other means of identification

Product number -
Other names Oxazole-4-carbaldehyde

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:118994-84-6 SDS

118994-84-6Relevant articles and documents

Photochemical approach to functionalized benzobicyclo[3.2.1]octene structures via fused oxazoline derivatives from 4-and 5-(o-vinylstyryl) oxazoles

agud, Ivana,Boiae, Simona,Mariniae, eljko,indler-Kulyk, Marija

, p. 2222 - 2229 (2014)

Novel cis/trans-4- and cis/trans -5-(2-vinylstyryl)oxazoles have been synthesized by Wittig reactions from the diphosphonium salt of α,α'- o -xylene dibromide, formaldehyde and 4- and 5-oxazolecarbaldehydes, respectively. In contrast, trans -5-(2-vinylsty

Synthesis and structure-activity relationships of bengazole A analogs

Mulder, Roger J.,Shafer, Cynthia M.,Dalisay, Doralyn S.,Molinski, Tadeusz F.

body text, p. 2928 - 2930 (2010/01/16)

Analogs of the potent antifungal agent, bengazole A, were prepared and evaluated against Candida spp. in both microbroth dilution and disk diffusion assays.

BICYCLONONENE DERIVATIVES AS RENIN INHIBITORS

-

Page/Page column 34, (2008/06/13)

The invention relates to novel bicyclononene derivatives of Formula (I); and the use thereof as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as inhibitors of renin.

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