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5-METHYL-2-PHENYL-1,3-OXAZOLE-4-CARBALDEHYDE is a chemical compound that belongs to the oxazole family, characterized by a five-membered ring containing one oxygen and one nitrogen atom. It is a yellowish liquid with a high boiling point and is known for its unique structure and reactivity, making it a versatile intermediate in the synthesis of various pharmaceuticals, agrochemicals, and natural products. 5-METHYL-2-PHENYL-1,3-OXAZOLE-4-CARBALDEHYDE also exhibits antimicrobial and antioxidant properties, which contribute to its potential therapeutic applications. However, it is important to handle 5-METHYL-2-PHENYL-1,3-OXAZOLE-4-CARBALDEHYDE with care due to its volatility and potential toxicity when exposed to high temperatures or inhaled.

70170-23-9

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70170-23-9 Usage

Uses

Used in Pharmaceutical Industry:
5-METHYL-2-PHENYL-1,3-OXAZOLE-4-CARBALDEHYDE is used as an intermediate in the synthesis of various pharmaceuticals for its unique structure and reactivity, enabling the production of a wide range of compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 5-METHYL-2-PHENYL-1,3-OXAZOLE-4-CARBALDEHYDE is utilized as an intermediate in the development of agrochemicals, taking advantage of its chemical properties to create effective products for agricultural use.
Used in Natural Products Synthesis:
5-METHYL-2-PHENYL-1,3-OXAZOLE-4-CARBALDEHYDE is employed as an intermediate in the synthesis of natural products, leveraging its unique structure to produce compounds that can be used in various applications within the industry.
Used for Antimicrobial Applications:
Due to its antimicrobial properties, 5-METHYL-2-PHENYL-1,3-OXAZOLE-4-CARBALDEHYDE is used in applications that require the inhibition of microbial growth, making it a potential candidate for use in various antimicrobial products.
Used for Antioxidant Applications:
The antioxidant properties of 5-METHYL-2-PHENYL-1,3-OXAZOLE-4-CARBALDEHYDE make it suitable for use in applications where protection against oxidative stress is required, such as in the development of certain pharmaceuticals or agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 70170-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,7 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70170-23:
(7*7)+(6*0)+(5*1)+(4*7)+(3*0)+(2*2)+(1*3)=89
89 % 10 = 9
So 70170-23-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2/c1-8-10(7-13)12-11(14-8)9-5-3-2-4-6-9/h2-7H,1H3

70170-23-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-METHYL-2-PHENYL-1,3-OXAZOLE-4-CARBALDEHYDE

1.2 Other means of identification

Product number -
Other names 5-Methyl-2-phenyloxazole-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:70170-23-9 SDS

70170-23-9Relevant academic research and scientific papers

1,3-Oxazole-isoniazid hybrids: Synthesis, antitubercular activity, and their docking studies

Katariya, Kanubhai D.,Shah, Shailesh R.

, (2020/01/25)

A series of novel N′-([2-aryl-5-methyl-1,3-oxazole-4-yl]methylene)isonicotino/nicotino hydrazides 10a-l were prepared by the condensation reaction of 2-aryl-5-methyl-1,3-oxazole-4-carbaldehydes 8a-f with the corresponding isonicotino/nicotino hydrazides 9

The synthesis and activity of oxazole and thiazole analogues of urocanic acid

Millan, David S.,Prager, Rolf H.,Brand, Catherine,Hart, Prue H.

, p. 811 - 816 (2007/10/03)

Direct exposure of human skin to sunlight leads to suppression of the immune system, believed to be mediated by urocanic acid. The synthesis of oxazole and thiazole analogues of urocanic acid is reported, as is their effect on biological markers of the hu

Thiazolidinedione derivatives as hypoglycemic agents

-

, (2008/06/13)

Hypoglycemic thiazolidine-2,4-dione derivatives of the formula STR1 wherein the dotted line represents a bond or no bond; V is --CH=CH--, --N=CH--, --CH=N--, S, O or NR; W is S, SO, SO2, SO2 NR1, NR1 SO2/s

Novel Thiazolidine-2,4-diones as Potent Euglycemic Agents

Hulin, Bernard,Clark, David A.,Goldstein, Steven W.,McDermott, Ruth E.,Dambek, Paul J.,et al.

, p. 1853 - 1864 (2007/10/02)

A new series of thiazolidine-2,4-diones was obtained by replacing the ether function of englitazone with various functional groups, i.e., a ketone, alcohol, or olefin moiety.These compounds lower blood glucose levels in the genetically obese and insulin-r

Thiazolidinedione derivatives as hypoglycemic agents

-

, (2008/06/13)

Hypoglycemic thiazolidine-2,4-dione derivatives of the formula wherein the dotted line represents a bond or no bond;, V is -CH=CH-, -N=CH-, -CH=N-, S, O or NR;, W is S, SO, SO2, SO2NR1, NR1SO2, CONR1 or NR1CO;, X is S, O,

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