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3300-67-2

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3300-67-2 Usage

General Description

o-CHLOROSTYRYL PHENYL KETONE is a chemical compound used in various industrial and research applications. It is a light yellow crystal powder with a molecular weight of 274.7. This chemical is commonly used as a photoinitiator in the production of polymers and adhesives. Its photoreactivity makes it useful in UV-curable inks, coatings, and dental materials. Additionally, o-CHLOROSTYRYL PHENYL KETONE has been studied for its potential as a photoinitiator in photodynamic therapy, a treatment for cancer and other diseases that involves the use of light-activated drugs. The compound is also known for its ability to generate singlet oxygen when exposed to light, which has implications for its use in various medical and industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 3300-67-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3300-67:
(6*3)+(5*3)+(4*0)+(3*0)+(2*6)+(1*7)=52
52 % 10 = 2
So 3300-67-2 is a valid CAS Registry Number.

3300-67-2Relevant articles and documents

Synthesis of 7-oxabicyclo[2.2.1]hept-5-en-2-yl derivatives and their screening for antimicrobial and antioxidant properties

Dhanapal, Ramu,Perumal, Paramasivan T.,Ramprasath, Chandrasekaran,Mathivanan, Narayanasamy

, p. 3599 - 3603 (2013)

Novel 7-oxabicyclo[2.2.1]hept-5-en-2-yl derivatives have been synthesized using boron trifluoride diethyl etherate catalyzed Diels-Alder reaction. This method presents considerable synthetic advantages in terms of high atom economy, mild reaction conditio

Facile microwave-assisted synthesis and antitubercular evaluation of novel aziridine derivatives

Sarojini, Perumal,Jeyachandran, Malaichamy,Sriram, Dharmarajan,Ranganathan, Palraj,Gandhimathi

, (2021/02/26)

Novel 2-(aryloxymethyl)aziridines and 2-((3-aryl-1-phenylallyloxy)methyl)aziridine derivatives were prepared via ring-opening reaction of epoxides. The synthesized derivatives were characterized by using elemental analysis (EA), FT-IR, 13C NMR, and 1H NMR. The in vitro antitubercular activities of the synthesized compounds were evaluated against Mycobacterium tuberculosis H37Rv (MTB H37Rv) strain using MTT-MABA assay. All the aziridine derivatives exhibited improved persuasive antitubercular activity against MTB H37Rv in comparison with standard drugs. Among the tested compounds, 2-(naphthalene-1-yloxy) methyl aziridine (5b), 2-(naphthalene-2-yloxy)methylaziridine (5c), 2-(m-tolyloxymethyl)aziridine (5e), 2-(3-(4-methoxyphenyl)-1-phenylalloxy)methylaziridine (12b) and 2-(3-(2-chlorophenyl)-1-phenylallyloxy)methylaziridine (12c) revealed promising activity against MTB H37Rv. Specifically, compound 5b and 12 b showed three-times more active (MIC = 0.5 μg/mL) than the standard drugs ethambutol (MIC = 1.56 μg/mL) and ciprofloxacin (MIC = 1.56 μg/mL).

Multi-target weapons: diaryl-pyrazoline thiazolidinediones simultaneously targeting VEGFR-2 and HDAC cancer hallmarks

C S, Ramaa,Kumar, Alan P.,Meyer-Almes, Franz-Josef,Safuan, Sabreena,Schweipert, Markus,Tilekar, Kalpana,Upadhyay, Neha

, p. 1540 - 1554 (2021/10/26)

In anticancer drug discovery, multi-targeting compounds have been beneficial due to their advantages over single-targeting compounds. For instance, VEGFR-2 has a crucial role in angiogenesis and cancer management, whereas HDACs are well-known regulators o

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