455256-35-6 Usage
Description
(AzidoMethyl)-cyclopentane is a chemical compound characterized by a cyclopentane ring with a methyl group and an azide group attached to it. The azide group, which consists of three nitrogen atoms, is known for its high reactivity. (AzidoMethyl)-cyclopentane is potentially useful in organic synthesis and serves as a precursor for various functionalized cyclopentane derivatives. Due to its explosive nature, (AzidoMethyl)-cyclopentane must be handled with caution, and proper safety measures are essential when working with it in a laboratory setting.
Uses
Used in Organic Synthesis:
(AzidoMethyl)-cyclopentane is used as a building block for the synthesis of various organic compounds. Its unique structure, featuring a cyclopentane ring and a reactive azide group, allows for the creation of a wide range of functionalized cyclopentane derivatives.
Used in Pharmaceutical Industry:
(AzidoMethyl)-cyclopentane is used as a precursor for the development of pharmaceutical compounds. The reactivity of the azide group enables the formation of new bonds and the synthesis of complex molecules with potential therapeutic applications.
Used in Chemical Research:
(AzidoMethyl)-cyclopentane is utilized as a research tool in the field of chemistry, particularly in the study of reaction mechanisms and the development of new synthetic methods. Its high reactivity and unique structure make it an interesting subject for scientific investigation.
Used in Material Science:
(AzidoMethyl)-cyclopentane can be employed in the development of novel materials, such as polymers and composites, with specific properties. The azide group's reactivity allows for the creation of new linkages and the modification of material characteristics.
Safety Precautions:
Due to the explosive nature of (AzidoMethyl)-cyclopentane, it is crucial to follow proper safety measures when handling this compound. This includes using appropriate protective equipment, working in a well-ventilated area, and adhering to established laboratory safety protocols.
Check Digit Verification of cas no
The CAS Registry Mumber 455256-35-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,5,2,5 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 455256-35:
(8*4)+(7*5)+(6*5)+(5*2)+(4*5)+(3*6)+(2*3)+(1*5)=156
156 % 10 = 6
So 455256-35-6 is a valid CAS Registry Number.
455256-35-6Relevant articles and documents
P-benzoquinone diazide core skeleton derivative as well as preparation method and application thereof
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Paragraph 0046; 0146-0150, (2020/03/17)
The invention relates to a p-benzoquinone diazide core skeleton derivative and a preparation method and application, thereof, belongs to. the field of organic chemistry, and can effectively treat-ovarian-ovarian cancer-carcinoma STAT3-ovarian, cancer-ATG4
SPIRO-LACTAM NMDA RECEPTOR MODULATORS AND USES THEREOF
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Paragraph 00317; page 130, (2014/08/19)
Disclosed are compounds having enhanced potency in the modulation of NMDA receptor activity. Such compounds are contemplated for use in the treatment of conditions such as depression and related disorders. Orally available formulations and other pharmaceutically acceptable delivery forms of the compounds, including intravenous formulations, are also disclosed.
An unexpected example of protein-templated click chemistry
Suzuki, Takayoshi,Ota, Yosuke,Kasuya, Yuki,Mutsuga, Motoh,Kawamura, Yoko,Tsumoto, Hiroki,Nakagawa, Hidehiko,Finn,Miyata, Naoki
supporting information; experimental part, p. 6817 - 6820 (2010/12/19)
(Figure Presented) It all happened with a click: In a search for histone deacetylase (HDAC) inhibitors using in situ click chemistry, the first example of protein-Cu acceleration of the azide-alkyne cycloaddition reaction was uncovered. The copper center
