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Trityl thiocyanate, also known as triphenylmethyl thiocyanate, is an organic compound with the chemical formula C19H15NS. It is a colorless crystalline solid that is soluble in organic solvents such as ethanol and dichloromethane. Trityl thiocyanate is primarily used as a protecting group in organic synthesis, particularly for the protection of alcohols and amines. It forms a stable and easily removable protecting group, which is crucial in multi-step synthesis processes. The compound is also employed as a reagent in various chemical reactions, including the detection of nucleophiles and the synthesis of trityl ethers. Due to its reactivity and stability, trityl thiocyanate plays a significant role in the field of organic chemistry, particularly in the development of pharmaceuticals and other complex organic molecules.

35036-90-9

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35036-90-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35036-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,3 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35036-90:
(7*3)+(6*5)+(5*0)+(4*3)+(3*6)+(2*9)+(1*0)=99
99 % 10 = 9
So 35036-90-9 is a valid CAS Registry Number.

35036-90-9Relevant academic research and scientific papers

Single C-F Transformations of o-Hydrosilyl Benzotrifluorides with Trityl Compounds as All-in-One Reagents

Idogawa, Rika,Kim, Youngchan,Shimomori, Ken,Hosoya, Takamitsu,Yoshida, Suguru

supporting information, p. 9292 - 9297 (2020/11/30)

A facile method to prepare difluoromethylenes, including α,α-difluorobenzyl chlorides, by single C-F transformations of benzotrifluorides is disclosed. The C-F cleavage followed by chlorination proceeded smoothly using trityl chloride through the generation of trityl cation as an activator and chloride anion as a nucleophile. Diverse difluoromethylenes such as difluorobenzyl ethers were efficiently prepared by virtue of the good versatility of the resulting chloro and fluorosilyl groups.

2-Chloro-1-methylpyridinium iodide, an efficient reagent for the conversion of alcohols into alkyl thiocyanates both under solvent and solvent-free conditions

Mokhtari, Babak,Azadi, Roya,Mardani, Edris

experimental part, p. 491 - 493 (2012/02/01)

A new application of the Mukaiyama reagent for the simple phosphine-free conversion of alcohols into the corresponding alkyl thiocyanates is described. This transformation can be achieved either in acetonitrile or under solvent-free conditions and the products obtained in good to excellent yields. The solvent-free procedure described here is the first report on the solvent-free thiocyanation of alcohols.

Nucleophilic Substitution Reactions of Alkyl Halides By Using New Polymer-Supported Reagents Containing Hemin

Saito, Kiyoshi,Harada, Kaoru

, p. 2562 - 2566 (2007/10/02)

A new polymer reagent consisting of hemin, divinylbenzene, and 2-methyl-5-vinylpyridine was synthesized by suspension copolymerization.Substitution reactions of primary, secondary, and tertiary alkyl halides with the hemin copolymer combined with cyanide, azide, and thiocyanate ions were given satisfactory yields.This reaction mechanism was revealed to be a SNi type on the basis of stereochemical study.The hemin copolymer was not only a polymer-supported reagent with functional capabilities, but also served to separate the product from the reaction mixture.

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