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1,3-Benzenedimethanethiol, 2-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78007-12-2

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78007-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78007-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,0 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78007-12:
(7*7)+(6*8)+(5*0)+(4*0)+(3*7)+(2*1)+(1*2)=122
122 % 10 = 2
So 78007-12-2 is a valid CAS Registry Number.

78007-12-2Relevant academic research and scientific papers

Synthesis of dibenzopyrenes and pyrenes via photolytic sulfur extrusion and intramolecular cross-coupling reactions of dithia[3.3] (1,3)naphthalenophanes and dithia[3.3]metacyclophanes

Ashram,Miller,Bridson,Georghiou

, p. 6476 - 6484 (1997)

The syntheses of several substituted dithia[3.3]metacyclophanes and dithia[3.3](1,3)naphthalenophanes are reported and their photolyses in triethyl or trimethyl phosphite are described. Under these conditions, the corresponding tetrahydrodibenzopyrenes and tetrahydropyrenes are produced in a one-pot procedure when the precursor dithianaphthalenophanes and dithiacyclophanes possess at least one intraannular methoxyl group. A mechanism with supporting evidence is proposed to account for these results. Structural determinations of the four isomeric 11,22-dimethoxy-2,13- dithia[3.3](1,3)naphthalenophanes by NMR and X-ray single-crystal diffraction studies are also described. The syntheses of the novel anti-transoid- and anti-cisoid-[2.2](1,3)naphthalenophanes are also described.

Homothiacalix[4]arenes: Synthetic exploration and solid-state structures

Thomas, Joice,Van Hecke, Kristof,Robeyns, Koen,Van Rossom, Wim,Sonawane, Mahendra P.,Van Meervelt, Luc,Smet, Mario,Maes, Wouter,Dehaen, Wim

supporting information; experimental part, p. 10339 - 10349 (2011/10/13)

Homothiacalix[n]arenes have been largely underexposed compared with related (homo)heteracalixarenes, although their inherent structural features are particularly attractive for supramolecular host-guest chemistry. In this contribution, the synthetic macro

Synthesis and conformational studies of 9-methoxy- and 9-methyl- 2,11-dithia[3.3]metacyclophanes

Shimizu, Tomoe,Maeda, Takayuki,Hida, Katsuhiro,Yamato, Takehiko

scheme or table, p. 515 - 519 (2010/01/16)

A series of 9-methoxy- and 9-methyl-2,11-dithia[3.3]metacyclophanes are obtained by the coupling reaction of the corresponding 1,3-bis(bromomethyl) benzenes and bis(sulfanylmethyl)benzenes in ethanol under the high dilution conditions. The conformational

syn/anti-Konformere und -Umlagerungen intra- und extraanular substituierter Dithiametacyclophane

Boeckmann, Klaus,Voegtle, Fritz

, p. 1065 - 1073 (2007/10/02)

New dithiametacyclophanes (Table 2) have been synthesized and their conformations determined.The dependence of extra- and intraanular substituents, especially methoxy, amino and phenyl groups, are discussed.The barriers of the thermal rearrangement o

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