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4-(But-3-en-1-yloxycarbonyl)benzoic acid is a carboxylic acid derivative with the molecular formula C13H12O4. It features a benzoic acid group and a but-3-en-1-yloxycarbonyl group, which endows it with unique structural and reactive properties. This chemical compound is a versatile building block in organic synthesis and pharmaceutical research, utilized for the creation of a variety of compounds.

62680-74-4

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62680-74-4 Usage

Uses

Used in Organic Synthesis:
4-(But-3-en-1-yloxycarbonyl)benzoic acid is used as a building block for the synthesis of various organic compounds. Its unique structure allows it to be a key component in the formation of complex organic molecules, contributing to the advancement of organic chemistry.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-(But-3-en-1-yloxycarbonyl)benzoic acid is used as a building block for the development of new pharmaceuticals. Its reactivity and structural features make it a valuable component in the synthesis of potential drug candidates, aiding in the discovery of novel therapeutic agents.
Used as a Reagent in the Preparation of Esters:
4-(But-3-en-1-yloxycarbonyl)benzoic acid is utilized as a reagent in the preparation of esters, which are important intermediates in organic chemistry. Its ability to form esters broadens its applications in the synthesis of a wide range of organic compounds.
Used in the Preparation of Other Organic Compounds:
Beyond its role in ester synthesis, 4-(But-3-en-1-yloxycarbonyl)benzoic acid is also employed in the preparation of other organic compounds. Its versatility in organic reactions makes it a valuable tool in the synthesis of various organic molecules, contributing to the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 62680-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,8 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62680-74:
(7*6)+(6*2)+(5*6)+(4*8)+(3*0)+(2*7)+(1*4)=134
134 % 10 = 4
So 62680-74-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O4/c1-2-3-8-16-12(15)10-6-4-9(5-7-10)11(13)14/h2,4-7H,1,3,8H2,(H,13,14)

62680-74-4SDS

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 4-but-3-enoxycarbonylbenzoic acid

1.2 Other means of identification

Product number -
Other names 4-(But-3-en-1-yloxycarbonyl)benzoic 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:62680-74-4 SDS

62680-74-4Relevant academic research and scientific papers

Amorphous Pure Organic Polymers for Heavy-Atom-Free Efficient Room-Temperature Phosphorescence Emission

Ma, Xiang,Xu, Chao,Wang, Jie,Tian, He

supporting information, p. 10854 - 10858 (2018/08/21)

Pure organic, heavy-atom-free room-temperature phosphorescence (RTP) materials have attracted much attention and have potential applications in photoelectric and biochemical material fields owing to their rich excited state properties. They offer long luminescent lifetime, diversified design, and facile preparation. However, recent achievements of efficient phosphorescence under ambient conditions mainly focus on ordered crystal lattices or embedding into rigid matrices, which require strict growth conditions and have poor reproducibility. Herein, we developed a concise approach to give RTP with a decent quantum yield and ultralong phosphorescence lifetime in the amorphous state by radical binary copolymerization of acrylamide and different phosphors with oxygen-containing functional groups. The cross-linked hydrogen-bonding networks between the polymeric chains immobilize phosphors to suppress non-radiative transitions and provide a microenvironment to shield quenchers.

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