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Tert-Butyl cyclohexyl sulfide is an organic compound with the chemical formula C10H20S. It is a colorless liquid at room temperature and has a molecular weight of 176.33 g/mol. tert-Butyl cyclohexyl sulfide is characterized by a tert-butyl group (a methyl group attached to a carbon atom that is already bonded to three other carbon atoms) and a cyclohexyl group (a six-membered ring structure similar to cyclohexane) connected by a sulfur atom, forming a sulfide bond. Tert-Butyl cyclohexyl sulfide is used as a synthetic intermediate in the production of various organic compounds and pharmaceuticals, and it is also employed as a reagent in organic synthesis. Due to its chemical structure, it exhibits unique properties such as stability and reactivity, making it a valuable component in various chemical processes.

7133-23-5

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7133-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7133-23-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7133-23:
(6*7)+(5*1)+(4*3)+(3*3)+(2*2)+(1*3)=75
75 % 10 = 5
So 7133-23-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H20S/c1-10(2,3)11-9-7-5-4-6-8-9/h9H,4-8H2,1-3H3

7133-23-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butylsulfanylcyclohexane

1.2 Other means of identification

Product number -
Other names Sulfide,tert-butyl cyclohexyl

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:7133-23-5 SDS

7133-23-5Downstream Products

7133-23-5Relevant academic research and scientific papers

Zn- And Cu-catalyzed coupling of tertiary alkyl bromides and oxalates to forge challenging C?O, C?S, and C?N bonds

Gong, Yuxin,Zhu, Zhaodong,Qian, Qun,Tong, Weiqi,Gong, Hegui

supporting information, p. 1005 - 1010 (2021/02/01)

We describe here the facile construction of sterically hindered tertiary alkyl ethers and thioethers via the Zn(OTf)2catalyzed coupling of alcohols/phenols with unactivated tertiary alkyl bromides and the Cu(OTf)2-catalyzed thiolation of unactivated tertiary alkyl oxalates with thiols. The present protocol represents one of the most effective unactivated tertiary C(sp3)? heteroatom bond-forming conditions via readily accessible Lewis acid catalysis that is surprisingly less developed.

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.

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