14315-14-1 Usage
Description
5-Methylthianaphthene, also known as 5-Methylbenzo[b]thiophene, is an organic compound characterized by its white, low melting mass. It belongs to the class of thianaphthenes, which are fused thiophene and naphthene structures. 5-Methylthianaphthene is of interest due to its unique chemical properties and potential applications in various fields.
Uses
Used in Proteomics Research:
5-Methylthianaphthene is used as a substituted thiophene in proteomics research. Its unique chemical structure allows it to be a valuable tool for studying protein-protein interactions, protein function, and other aspects of proteomics. The compound's properties make it suitable for use in the development of new methodologies and techniques in this field.
Used in Chemical Synthesis:
Due to its distinctive structure, 5-Methylthianaphthene can be utilized as a building block or intermediate in the synthesis of various organic compounds. Its presence in the final products can contribute to the development of new materials with specific properties, such as improved stability, reactivity, or selectivity.
Used in Pharmaceutical Industry:
5-Methylthianaphthene may also find applications in the pharmaceutical industry, where its unique chemical properties could be harnessed for the development of new drugs or drug candidates. Its potential use in drug discovery and design could lead to the creation of novel therapeutic agents with improved efficacy and selectivity.
Used in Material Science:
The compound's distinctive structure and properties make it a candidate for use in material science, where it could be employed in the development of new materials with specific characteristics. These materials could have applications in various industries, such as electronics, aerospace, or automotive, where unique properties like thermal stability, electrical conductivity, or mechanical strength are desired.
Check Digit Verification of cas no
The CAS Registry Mumber 14315-14-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,1 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14315-14:
(7*1)+(6*4)+(5*3)+(4*1)+(3*5)+(2*1)+(1*4)=71
71 % 10 = 1
So 14315-14-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H8S/c1-7-2-3-9-8(6-7)4-5-10-9/h2-6H,1H3
14315-14-1Relevant articles and documents
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Tarbell et al.
, p. 1643 (1945)
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Dioxazolones as masked ester surrogates in the Pd(ii)-catalyzed direct C-H arylation of 6,5-fused heterocycles
Saxena, Paridhi,Maida, Neha,Kapur, Manmohan
, p. 11187 - 11190 (2019/09/30)
A simple and effective Pd(ii)-catalyzed regioselective C(2)-H arylation of 6,5-fused heterocycles with dioxazolones as a masked ester surrogate under mild conditions is reported. The significance of the arylation is highlighted by the new reactivity demonstrated in dioxazolones via proximal C-H activation of the cyclic carbonate of the hydroxamic acid functionality under protic conditions.
C-benzo five-membered heteroaromatic aryl glucoside derivative as well as preparation method and application thereof
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Paragraph 0077; 0078, (2016/10/08)
The invention discloses a C-benzo five-membered heteroaromatic aryl glucoside derivative shown in the general formula (I) (in the description), a preparation method of the derivative or an intermediate of the derivative, as well as application of the derivative. In the general formula (I), R, R1, R2, R3, R4, X and Y are defined in the description. The C-benzo five-membered heteroaromatic aryl glucoside derivative is novel in structure, has quite strong inhibitory activity on SGLT-2, has high selection ratio for SGLT-1 and SGLT-2, and can be used for preparing drugs for treating and preventing diseases relevant to SGLT-2.
