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87716-84-5

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87716-84-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87716-84-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,1 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87716-84:
(7*8)+(6*7)+(5*7)+(4*1)+(3*6)+(2*8)+(1*4)=175
175 % 10 = 5
So 87716-84-5 is a valid CAS Registry Number.

87716-84-5Downstream Products

87716-84-5Relevant academic research and scientific papers

One-pot Metal-free Synthesis of Benzyl Alkyl Sulfides

Lu, Xiaogang,Wang, Hongmei,Gao, Runli,Pei, Chengxin

, p. 45 - 52 (2015/10/29)

The synthesis of sulfides is important in various fields. This paper reports an efficient, odorless, and viable protocol for the base-mediated synthesis of benzyl alkyl sulfides using thiourea. The reactions were carried out under transition-metal-free co

Synthesis of a wide range of thioethers by indium triiodide catalyzed direct coupling between alkyl acetates and thiosilanes

Nishimoto, Yoshihiro,Okita, Aya,Yasuda, Makoto,Baba, Akio

supporting information; experimental part, p. 1846 - 1849 (2012/06/18)

An indium triiodide-catalyzed substitution of the acetoxy group in alkyl acetates with thiosilanes provides access to a variety of thioethers. The method is efficient for a wide scope of acetates such as primary alkyl, secondary alkyl, tertiary alkyl, allylic, benzylic, and propargylic acetates.

Boron trifluoride monohydrate catalyzed one-flask preparation of sulfides from carbonyl compounds with thiols and triethylsilane

Olah,Wang,Trivedi,Prakash

, p. 465 - 4466 (2007/10/02)

Boron trifluoride monohydrate catalyzed thiolation of aldehydes and ketones with thiols and triethylsilane to the corresponding sulfides was carried out in good to excellent yields.

Nucleophilic Substitution of Alkyl Halides by Zinc Salts: Part 4-Synthesis of Thioethers and Thiolesters

Rajanikanth, B.,Ravindranath, B.

, p. 1043 - 1045 (2007/10/02)

A variety of alkyl halides including tertiary alkyl halides react smoothly with the zinc salts of thiols and thiolcarboxylic acids yielding thioethers and thiolesters.

Chemistry of Amine-Boranes. Part 10. Synthesis of Sulphides from Dithioacetals using Pyridine-Borane in Acid

Kikugawa, Yasuo

, p. 609 - 610 (2007/10/02)

The synthesis of sulphides from dithioacetals in trifluoroacetic acid or in dichloromethane in the presence of aluminium chloride with pyridine-borane is described.

A NEW SYNTHESIS OF SULFIDES FROM THIOLS AND ALDEHYDES OR KETONES WITH PYRIDINE-BORANE IN TRIFLUOROACETIC ACID

Kikugawa, Yasuo

, p. 1157 - 1158 (2007/10/02)

A mixture of thiols and aldehydes or ketones was converted into sulfides with pyridine-borane in trifluoroacetic acid.

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