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BENZOIC ACID, 4-HEPTYL-, 1,3,4-OXADIAZOLE-2,5-DIYLDI-4,1-PHENYLENE ESTER is a complex organic chemical compound that combines the properties of benzoic acid with the unique characteristics of 1,3,4-oxadiazole-2,5-diyldi-4,1-phenylene ester. BENZOIC ACID, 4-HEPTYL-, 1,3,4-OXADIAZOLE-2,5-DIYLDI-4,1-PHENYLENE ESTER exhibits a diverse range of potential applications due to its structural composition, which includes a benzoic acid moiety and an oxadiazole-phenylene ester linkage. The presence of these functional groups suggests that it could be utilized in various industries, including food preservation, fragrance production, pharmaceuticals, and the development of advanced materials.

279675-92-2

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279675-92-2 Usage

Uses

Used in Food Preservation Industry:
BENZOIC ACID, 4-HEPTYL-, 1,3,4-OXADIAZOLE-2,5-DIYLDI-4,1-PHENYLENE ESTER is used as a preservative agent for its ability to inhibit the growth of microorganisms, thereby extending the shelf life of food products. The benzoic acid component contributes to its antimicrobial properties, making it a valuable addition to the food industry.
Used in Fragrance Production:
In the fragrance industry, BENZOIC ACID, 4-HEPTYL-, 1,3,4-OXADIAZOLE-2,5-DIYLDI-4,1-PHENYLENE ESTER is used as a scent ingredient due to its aromatic properties. The heptyl chain attached to the benzoic acid provides a unique olfactory profile, which can be utilized in creating various fragrances for personal care and household products.
Used in Pharmaceutical Industry:
The 1,3,4-oxadiazole-2,5-diyldi-4,1-phenylene ester component of BENZOIC ACID, 4-HEPTYL-, 1,3,4-OXADIAZOLE-2,5-DIYLDI-4,1-PHENYLENE ESTER may have potential applications in the pharmaceutical industry. The oxadiazole ring is known for its diverse biological activities, and when combined with the phenylene ester linkage, it could be used in the development of new drugs with specific therapeutic properties.
Used in Advanced Materials Industry:
BENZOIC ACID, 4-HEPTYL-, 1,3,4-OXADIAZOLE-2,5-DIYLDI-4,1-PHENYLENE ESTER may also find use in the development of advanced materials due to its unique structural features. The combination of benzoic acid and oxadiazole-phenylene ester could be employed in the synthesis of new polymers, coatings, or other materials with specialized properties for various applications, such as in electronics, automotive, or aerospace industries.

Check Digit Verification of cas no

The CAS Registry Mumber 279675-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,9,6,7 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 279675-92:
(8*2)+(7*7)+(6*9)+(5*6)+(4*7)+(3*5)+(2*9)+(1*2)=212
212 % 10 = 2
So 279675-92-2 is a valid CAS Registry Number.

279675-92-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[5-[4-(4-heptylbenzoyl)oxyphenyl]-1,3,4-oxadiazol-2-yl]phenyl] 4-heptylbenzoate

1.2 Other means of identification

Product number -
Other names (1,3,4-Oxadiazole-2,5-diyl)bis(4,1-phenylene) bis(4-heptylbenzoate)

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:279675-92-2 SDS

279675-92-2Downstream Products

279675-92-2Relevant academic research and scientific papers

Enantioselective segregation in achiral nematic liquid crystals

Goertz, Verena,Goodby, John W.

, p. 3262 - 3264 (2007/10/03)

The elusive biaxial nematic liquid crystal phase was recently discovered in a family of substituted oxadiazoles. Our investigations of these materials show that the achiral biaxial nematic phase can segregate into chiral domains of opposite handedness, th

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