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118637-72-2

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118637-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118637-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,3 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 118637-72:
(8*1)+(7*1)+(6*8)+(5*6)+(4*3)+(3*7)+(2*7)+(1*2)=142
142 % 10 = 2
So 118637-72-2 is a valid CAS Registry Number.

118637-72-2Downstream Products

118637-72-2Relevant academic research and scientific papers

A close-packed, highly insulating organic thin monolayer on Si(111)

Tanaka, Kentaro,Tanaka, Taishi,Hasegawa, Takeshi,Shionoya, Mitsuhiko

, p. 440 - 441 (2008)

A long-chain dialkylated olefin, 2C18 was found to form a close-packed, highly insulating self-assembled monolayer (SAM) on Si(111) via Si-C bond formation. The IR absorption spectra of the 2C18-SAM show that the alkyl chains are densely packed with an all-trans conformation. The threshold voltage to initiate the scanned probe oxidation (SPO) of the 2C18-SAM-covered Si(111) was ca. 9V, which is much higher than the previously reported voltages for organic monolayers on Si or SiO2/Si substrates. Copyright

Synthesis and Characterization of Carboxylic Acids Bearing Poly(ethylene glycol) Chains

Satou, Motoi,Fujihara, Tetsuaki,Terao, Jun,Tsuji, Yasushi

, p. 556 - 559 (2018)

Carboxylic acids 1a and 1b bearing three poly(ethylene glycol) (PEG) chains and carboxylic acid 1c bearing one PEG chain were designed and synthesized. The carboxylic acids 1a - c were fully characterized by NMR and ESI-HRMS analyses. In a Pd-catalyzed ae

Practical heavy fluorous tag for carbohydrate synthesis with minimal chromatographic purification

Goto, Kohtaro,Mizuno, Mamoru

scheme or table, p. 6539 - 6541 (2011/02/22)

A practical heavy fluorous tag 5 bound to a benzylic linker was prepared and applied to carbohydrate synthesis. The fluorous tag 5 was readily introduced to the desired hydroxyl group and carboxyl group by using various methods. Synthesis of the oligosacc

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