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1-Butanol, 4-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60012-67-1

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60012-67-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60012-67-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,1 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60012-67:
(7*6)+(6*0)+(5*0)+(4*1)+(3*2)+(2*6)+(1*7)=71
71 % 10 = 1
So 60012-67-1 is a valid CAS Registry Number.

60012-67-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(benzenesulfonyl)butan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Butanol,4-(phenylsulfonyl)

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:60012-67-1 SDS

60012-67-1Relevant academic research and scientific papers

Sulfone derivatives as 5-HT7 receptor ligands

-

Page/Page column 8, (2010/02/09)

The present invention relates to sulfone derivatives of formula (I): Ar—SO2—CR2R3-L-N(R1)2??I wherein Ar, L, R1, R2 and R3 are as defined herein, and pharmaceutically

A FACILE SYNTHESIS OF SPIROKETALS

Brimble, Margaret A.,Officer, David L.,Williams Geoffrey M.

, p. 3609 - 3612 (2007/10/02)

A convenient synthetic approach to spiroketals based on the addition of α-sulfonylcarbanions to lactones is described.

Elimination and Addition Reactions. Part 44. Eliminative Fission of Cycloalkanols

Bury, Adrian,Earl, Harold A.,Stirling, Charles J. M.

, p. 1281 - 1288 (2007/10/02)

Activation parameters for the fission of cyclopropanols and cyclobutanols with phenyl groups α or phenylthio or phenylsulphonyl groups β to the hydroxy group have been obtained.The results show very large differences in reactivity between cyclopropanols and cyclobutanols; such differences are also found in energy profiles for the opening of cycloalkoxide ions obtained by using MINDO3.The results are entirely compatible with other three-membered/four-membered ring comparisons and the role of strain in these systems is discussed.Attempts to extend the well established enforced catalysis of cycloalkanol ring fission to electrophiles other than Broensted acids have failed.

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