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3,7-dimethyldibenzo[b,d]thiophene is an organic compound with the molecular formula C14H12S. It is a derivative of dibenzo[b,d]thiophene, a heterocyclic aromatic compound consisting of two benzene rings fused to a thiophene ring. The two methyl groups attached at the 3 and 7 positions provide additional steric hindrance and electronic effects to the molecule. 3,7-dimethyldibenzo[b,d]thiophene is of interest in various fields, including materials science and organic chemistry, due to its unique electronic properties and potential applications in the synthesis of advanced materials and pharmaceuticals. It is typically synthesized through various chemical reactions and can be characterized using techniques such as nuclear magnetic resonance (NMR) and mass spectrometry.

1136-85-2

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1136-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1136-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1136-85:
(6*1)+(5*1)+(4*3)+(3*6)+(2*8)+(1*5)=62
62 % 10 = 2
So 1136-85-2 is a valid CAS Registry Number.

1136-85-2Downstream Products

1136-85-2Relevant academic research and scientific papers

Gallium Modified HUSY Zeolite as an Effective Co-support for NiMo Hydrodesulfurization Catalyst and the Catalyst's High Isomerization Selectivity

Zhou, Wenwu,Zhou, Yasong,Wei, Qiang,Du, Lin,Ding, Sijia,Jiang, Shujiao,Zhang, Yanan,Zhang, Qing

, p. 9369 - 9382 (2017)

The effects of metal-modified acidic co-supports on the hydrodesulfurization (HDS) activity and isomerization selectivity of highly refractory organosulfur compounds such as 4,6-dimethyldibenzothiophene have been investigated. Y zeolite crystals with high Si/Al ratios and small crystallite sizes were successfully synthesized by a new hydrothermal synthesis approach. The synthesized Y zeolite crystals were ion-exchanged and stabilized. The prepared samples were then modified with different gallium contents using an impregnation method to adjust their acidity properties, and these modified samples were used as co-supports for NiMo sulfide HDS catalysts. The catalyst containing 10 wt.% zeolite Y modified by 2 wt.% gallium (NiMo/2GaY-ASA-A) exhibited the highest HDS activity, with 4,6-dimethyldibenzothiophene (4,6-DMDBT) conversion nearly double the rate of the catalyst without zeolite at 563 K, 4.0 MPa and liquid hourly space velocity (LHSV) of 40 h?1. NiMo/2GaY-ASA-A also exhibited superior isomerization ability, with 3,4′-DMBP, 4,4′DMBP, and 3,6-DMDBT as the main products, indicating that the isomerization pathway was the main reaction route over NiMo/2GaY-ASA-A. The superior catalytic performance is related to the synergistic effect of the proper amount of medium and strong Br?nsted acid sites. The compounds 3,6-DMDBT and 3,7-DMDBT (isomers of 4,6-DMDBT) and 3,4,6-TMDBT and tetra-methyl-DBT (transmethyl products) were detected simultaneously in the HDS product of 4,6-DMDBT for the first time over NiMo/GaY-ASA-A catalysts. Finally, a new reaction network over NiMo/2GaY-ASA-A was proposed.

The Synthesis of All of the Dimethyldibenzothiophenes and Monoethyldibenzothiophenes

Tedjamulia, Marvin L.,Tominaga, Yoshinori,Castle, Raymond N.

, p. 1485 - 1495 (2007/10/02)

The synthesis of all four isomers of the monoethyldibenzothiophenes and all of the sixteen isomers of the dimethyldibenzothiophenes has been accomplished.

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