14315-14-1

Basic information

• Product Name: 5-Methylthianaphthene
• Synonyms: BUTTPARK 33\04-62;5-METHYL-1-BENZOTHIOPHENE;5-METHYLBENZO[B]THIOPHENE;5-METHYLBENZOTHIOPHENE;5-methylthianaphthene;Benzo[b]thiophene, 5-methyl-;Benzothiophene, 5-mehyl;5-Methylbenzobüthiophene, 96%
• CAS NO: 14315-14-1
• Molecular Formula: C₉H₈S
• Molecular Weight: 148.22
• EINECS: 238-256-2
• Product Categories: Thiophenes & Benzothiophenes;Thiophenes & Benzothiophenes
• Mol File: 14315-14-1.mol
• Article Data: 20

Chemical Properties

• Melting Point: 35-36 °C
• Boiling Point: 71-73°C 0,6mm
• Flash Point: 71-73°C/0.6mm
• Appearance: White/Low Melting Mass
• Density: 1,111 g/cm3
• Vapor Pressure: 0.0514mmHg at 25°C
• Refractive Index: 1.6150 (estimate)
• Storage Temp.: 2-8°C
• Water Solubility: Insoluble in water.
• BRN: 109866
• CAS DataBase Reference: 5-Methylthianaphthene(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Methylthianaphthene(14315-14-1)
• EPA Substance Registry System: 5-Methylthianaphthene(14315-14-1)

Safety Data

• Hazard Codes: Xn
• Statements: 36/37/38-22
• Safety Statements: 36/37/39-26-22
• Hazardous Substances Data: 14315-14-1(Hazardous Substances Data)

Usage

Chemical Properties

white low melting mass

Uses

5-Methylbenzo[b]thiophene is useful in substituted thiophene for proteomics research.

InChI:InChI=1/C9H8S/c1-7-2-3-9-8(6-7)4-5-10-9/h2-6H,1H3

Upstream product

• 65520-23-2 5-methyl-benzo[b]thiophen-3-ol 
• 1505-62-0 5-methyl-benzo[b]thiophene-2-carboxylic acid 
• 56639-88-4 5-methylbenzothiophen-3(2H)-one 
• 106-45-6 para-thiocresol 
• 74-86-2 acetylene 
• 103-19-5 di(p-tolyl) disulfide 
• 6007-83-6 2,3-thiophenedicarboxylic acid anhydride 
• 542-92-7 cyclopenta-1,3-diene 
• 51830-50-3 1,1-diethoxy-2-(4-methylphenylthio)ethane 
• 1199-06-0 6-methylthiocoumarin 
• 4923-87-9 5-bromobenzo[b]thiophene 
• 13061-96-6 dihydroxy-methyl-borane 
• 2032-35-1 Bromoacetaldehyde diethyl acetal 
• 13616-73-4 5-methyl-2-methylthiobenzaldehyde 

Downstream Products

• 10133-22-9 5-bromomethyl-benzo[b]thiophene 
• 10133-30-9 benzo[b]thiophene-5-carbaldehyde 
• 108012-20-0 5-methyl-3-phenylbenzo[b]thiophene 
• 82787-69-7 5-methylbenzothiophene-2-carboxylic acid methyl ester 
• 27035-41-2 5-Methylbenzothiophen-2-carbaldehyd 
• 22721-01-3 5-methyl-2-p-tolylbenzothiophen 
• 1505-62-0 5-methyl-benzo[b]thiophene-2-carboxylic acid 
• 16587-51-2 2-ethyl-5-methylbenzo[b]thiophene 
• 55164-43-7 5-methyl-2-phenylbenzothiophene 

Relevant articles and documents

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Dioxazolones as masked ester surrogates in the Pd(ii)-catalyzed direct C-H arylation of 6,5-fused heterocycles

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

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.