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4-Heptanol, 4-methylbenzenesulfonate is a chemical compound that can be described as a derivative of 4-heptanol, where a 4-methylbenzenesulfonate group has been attached to the hydroxyl group of the alcohol. 4-Heptanol, 4-methylbenzenesulfonate is an ester, formed by the reaction between 4-heptanol and 4-methylbenzenesulfonyl chloride. It is a colorless liquid with a molecular weight of approximately 222.31 g/mol. The compound is used in various applications, such as a solvent or a reagent in organic synthesis, and is known for its ability to form esters with other alcohols. It is important to handle 4-Heptanol, 4-methylbenzenesulfonate with care due to its potential irritant properties and to follow proper safety protocols when working with it.

4883-86-7

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4883-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4883-86-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,8 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4883-86:
(6*4)+(5*8)+(4*8)+(3*3)+(2*8)+(1*6)=127
127 % 10 = 7
So 4883-86-7 is a valid CAS Registry Number.

4883-86-7SDS

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 4-heptyltoluene-p-sulphonate

1.2 Other means of identification

Product number -
Other names 1-propylbutyl tosylate

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:4883-86-7 SDS

4883-86-7Relevant academic research and scientific papers

77Se NMR. Application of JSe-Se to the Analysis of Dialkyl Polyselenides

Eggert, Hanne,Nielsen, Ole,Henriksen, Lars

, p. 1725 - 1730 (2007/10/02)

Elemental selenium is partially reduced via either disproportionation or reaction with sodium methanolate and hydrazine in dipolar aprotic media.These reductions both give polyselenide ions with a known average chain length, Sen(2-) (3 /= n /

Nuclear Heptylation of Benzene and Naphthalene and Cyclopentylation of Toluene

Badr, M. Z. A.,El-Naggar, G. M.,Aly, M. M.,Fahmy, A. M.

, p. 961 - 964 (2007/10/02)

Thermal decomposition of 1-, 2-, 3- and 4-heptyltoluene-p-sulphonates in the presence of aromatic substrates like benzene or naphthalene at 130-35 deg, affords differently substituted α- and β-isomers in the case of naphthalene.Skeletal isomerisation of the alkyl group is observed where different isomeric 1-, 2-, 3- and 4-heptyl-aromatics are obtained.Also thermal decomposition of cyclopentylmethane sulphonate in the presence of toluene at 130-35 deg, furnishes the corresponding o-, m- and p-substituted toluenes.The isomers have been identified and estimated quantitatively by GLC.

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