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2,2′-disulfanediyldicyclohexanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86853-20-5

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86853-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86853-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,5 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86853-20:
(7*8)+(6*6)+(5*8)+(4*5)+(3*3)+(2*2)+(1*0)=165
165 % 10 = 5
So 86853-20-5 is a valid CAS Registry Number.

86853-20-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name racem.-bis-(trans-2-hydroxy-cyclohexyl)-disulfide

1.2 Other means of identification

Product number -
Other names racem.-Bis-(trans-2-hydroxy-cyclohexyl)-disulfid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:86853-20-5 SDS

86853-20-5Relevant academic research and scientific papers

An oxorhenium complex bearing a chiral cyclohexane-1-olato-2-thiolato ligand: Synthesis, stereochemistry, and theoretical study of parity violation vibrational frequency shifts

Saleh, Nidal,Bast, Radovan,Vanthuyne, Nicolas,Roussel, Christian,Saue, Trond,Darquié, Beno?t,Crassous, Jeanne

, p. 147 - 156 (2018/01/17)

In our effort towards measuring the parity violation energy difference between two enantiomers, a simple chiral oxorhenium complex 5 bearing enantiopure 2-mercaptocyclohexan-1-ol has been prepared as a potential candidate species. Vibrational circular dichroism revealed a chiral environment surrounding the rhenium atom, even though the rhenium is not a stereogenic center itself, and enabled to assign the (1S,2S)-(?) and (1R,2R)-(+) absolute configuration for 5. For both compound 5 and complex 4, previously studied by us and bearing a propane-2-olato-3-thiolato ligand, relativistic calculations predict parity violating vibrational frequency differences of a few hundreds of millihertz, above the expected sensitivity attainable by a molecular beam Ramsey interferometer that we are constructing.

A new stable modified borohydride reagent. Efficient reduction of different functional groups with sulfurated barium borohydride [Ba(BH2S3)2] in dry THF

Firouzabadi, Habib,Ghadami, Mahboobeh

, p. 83 - 98 (2007/10/03)

Barium and strontium sulfurated borohydrides, Ba(BH2S3)2,Sr(BH2S3) 2 the two newly introduced modified borohydride agents, are prepared from NaBH2S3 by metathesis reaction with BaCl2 and SrCl2 in good yields. Ba(BH2S3)2 is more stable and more reactive than Sr(BH2S3)2. The reducing ability of Ba(BH2S3)2 for the reduction of aldehydes, ketones, α,β-unsaturated carbonyl compounds, azides, nitro compounds, and cleavage of epoxides in dry THF is described.

Highly efficient, regio- and stereoselective ring opening of epoxides and thiiranes with Ce(OTf)4

Iranpoor,Shekarriz,Shiriny

, p. 347 - 366 (2007/10/03)

Ceric triflate, Ce(OTf)4 is used as an efficient catalyst for ring opening of epoxides in the presence of alcohols, water, and acetic acid. The reactions proceed with high regio and stereoselectivity and in excellent yields. The reaction of R(+) styrene oxide with methanol occurs with excellent optical purity. Ring opening of thiiranes in alcohols, water and acetic acid followed by dimerisation to the corresponding disulfides occur efficiently in the presence of this reagent. A mild method for the preparation of dithianes from thiiranes and Ce(OTf)4 is also described.

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