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2,5-dibromo-1,4-bis(methylthio)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84910-84-9

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84910-84-9 Usage

General Description

2,5-dibromo-1,4-bis(methylthio)benzene is a chemical compound with the molecular formula C10H10Br2S2. It is a yellow crystalline solid with a strong odor, and it is insoluble in water. 2,5-dibromo-1,4-bis(methylthio)benzene is primarily used as a building block or intermediate in the manufacture of various organic compounds, including pharmaceuticals, agrochemicals, and dyes. It is also used in the synthesis of advanced materials and as a reagent in organic chemistry reactions. The chemical properties of 2,5-dibromo-1,4-bis(methylthio)benzene make it a valuable tool for researchers and industry professionals in a wide range of applications. However, it is important to handle and store 2,5-dibromo-1,4-bis(methylthio)benzene in a safe and controlled manner, as it can be hazardous to human health and the environment if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 84910-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,1 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84910-84:
(7*8)+(6*4)+(5*9)+(4*1)+(3*0)+(2*8)+(1*4)=149
149 % 10 = 9
So 84910-84-9 is a valid CAS Registry Number.

84910-84-9Relevant academic research and scientific papers

Compound containing fused heterocycle structure, application of compound and organic electroluminescent device

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Paragraph 0139-0141, (2021/05/05)

The invention relates to the field of organic electroluminescent devices, and discloses a compound containing a fused heterocycle structure, an application of the compound and an organic electroluminescent device. The compound has the general formula structure shown in the formula (I); the compound has a high glass transition temperature, a high decomposition temperature and a high refractive index; and when the compound is applied to a covering layer on a device, the light extraction efficiency of the cathode can be improved, so that the luminous efficiency of the device is improved, and the service life of the device is prolonged.

Triphenylsilyl-linked benzothiophene derivative and organic light-emitting device using the same

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Paragraph 0045; 0046; 0047, (2017/08/02)

The invention provides a triphenylsilyl-linked benzothiophene derivative and an organic light-emitting device using the same and belongs to the technical field of organic photoelectric materials. The triphenylsilyl-linked benzothiophene derivative has a s

β-alkyl substituted dithieno[2,3-d;2′,3′-d′]benzo[1, 2-b;4,5-b′]dithiophene semiconducting materials and their application to solution-processed organic transistors

Kim, Jonggi,Yang, Changduk,Han, A-Reum,Oh, Joon Hak,Seo, Jung Hwa

, p. 3464 - 3472,9 (2020/08/24)

A novel highly π-extended heteroacene with four symmetrically fused thiophene-ring units and solubilizing substituents at the terminal β-positions on the central ring, dithieno[2,3-d;2′,3′-d′] benzo[1,2-b;4,5-b′]dithiophene (DTBDT) was synthesized via int

Conjugated ladder-type heteroacenes bearing pyrrole and thiophene ring units: Facile synthesis and characterization

Gao, Peng,Feng, Xinliang,Yang, Xiaoyin,Enkelmann, Volker,Baumgarten, Martin,Muellen, Klaus

supporting information; experimental part, p. 9207 - 9213 (2009/04/11)

(Chemical Equation Presented) Ladder-type heteroacenes containing pyrrole and thiophene rings, dibenzo[b,b′]thieno[2,3-f:5,4-f′]-carbazoles (DBTCZ, 1), and diindolo[3,2-b:2′,3′-h]benzo[1],2-b:4,5-b′] bis[1]benzothiophene (DIBBBT, 2), were facilely synthes

Dithia-s-indacene derivative

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Page/Page column 8-9, (2010/02/14)

A 1,5-dithia-s-indacene or 1,7-dithia-s-indacene derivative represented by general formula (1): wherein R1 and R2 each independently represents a hydrogen atom, an alkyl group or an alkoxy group; R3-R12 each ind

Sulfur analogues of psychotomimetic agents. 2. Analogues of (2,5-dimethoxy-4-methylphenyl)- and (2,5-dimethoxy-4-ethylphenyl)isopropylamine

Jacob III,Shulgin

, p. 746 - 752 (2007/10/02)

The two thio analogues of each of the well-known psychotomimetic drugs DOM [(2,5-dimethoxy-4-methylphenyl)isopropylamine] and DOET [(2,5-dimethoxy-4-ethylphenyl)isopropylamine] have been synthesized and pharmacologically evaluated in man. The 5-thio isome

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