Welcome to LookChem.com Sign In|Join Free
  • or
Cyclohexanone, 2-[(butylthio)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42557-89-1

Post Buying Request

42557-89-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

42557-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42557-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,5 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 42557-89:
(7*4)+(6*2)+(5*5)+(4*5)+(3*7)+(2*8)+(1*9)=131
131 % 10 = 1
So 42557-89-1 is a valid CAS Registry Number.

42557-89-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(butylsulfanylmethyl)cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2-butylsulfanylmethyl-cyclohexanone

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:42557-89-1 SDS

42557-89-1Relevant academic research and scientific papers

COMPLEX FORMATION OF D- AND F-ELEMENTS WITH SULPHUR ORGANIC COMPOUNDS IN EXTRAKTION EQUILIBRIA

Murinov, Yu. I.

, p. 65 - 110 (2007/10/02)

The regularities in reactivities of some mono- and polydentate organosulphur compounds have been established for complex formation with metal salts in extraction-sorption equilibria.Their reactivities have been shown to depend upon the spatial arrangement of donor centres in an extractant.New classes of polydentate extractants (keto sulphides, amino-sulphides, keto-aminosulphides) have been suggested. Chemical properties of coordinative extractions and sorptions have been investigated for d- and f-elements to be the most intrinsic for the above mentioned class.The keto group has been found to affect the electron density of sulphur in the keto sulphides, thus preventing undesirable redox reactions between an extractant and the isolated metal ion.The coordination character and properties of extracted and sorbated complexes of d- and f-elements with organosulphur compounds have been determined. The donor centres of polydentate organosulphur ligands in the process of complex formation with d- and f-elements have been detected by IR-, ESR-, PMR-, and Raman spectral analyses.

REACTIONS OF α-HETEROATOM-SUBSTITUTED ETHERS AND SULFIDES WITH SILYL ENOL ETHERS. CHEMOSELECTIVITY IN THE CLEAVAGE OF HETEROATOM-CARBON BONDS BY IODOTRIMETHYLSILANE AND TRIMETHYLSILYL TRIFLUOROMETHANESULFONATE

Hosomi, Akira,Sakata, Yasuyuki,Sakurai, Hideki

, p. 405 - 408 (2007/10/02)

Reactions of α-heteroatom substituted ethers and related compounds (R1R2CXY; X, Y = RO, RS and Cl) with silyl enol ethers and ketene silyl acetals took place in the presence of iodotrimethylsilane (Ia) and trimethylsilyl triflate (Ib) as a catalyst and factors influencing the activation of the heteroatom by I were examined.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 42557-89-1