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Benzenesulfonic acid, octyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13149-99-0

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13149-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13149-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,4 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13149-99:
(7*1)+(6*3)+(5*1)+(4*4)+(3*9)+(2*9)+(1*9)=100
100 % 10 = 0
So 13149-99-0 is a valid CAS Registry Number.

13149-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name octyl benzenesulfonate

1.2 Other means of identification

Product number -
Other names benzenesulfonic acid octyl ester

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:13149-99-0 SDS

13149-99-0Relevant academic research and scientific papers

CsF-Celite as an efficient heterogeneous catalyst for sulfonylation and desulfonylation of heteroatoms

Tamaddon, Fatemeh,Nasiri, Alireza,Farokhi, Somayeh

, p. 1477 - 1482 (2011)

CsF-Celite is found to be as an efficient reusable catalyst for sulfonylation and desulfonylation of heteroatoms. Sulfonamides and N-acylsulfonamides deprotect efficiently in the presence of CsF-Celite under solvent free conditions to give the free amines or amides in good to excellent yields.

Process for preparation of oxyglutaric acid ester derivatives

-

, (2008/06/13)

A process for preparing an oxyglutaric acid ester derivative of the formula: STR1 in which each of R1 and R2 is C1-5 alkoxy, C1-7 aralkyloxy, C7-9 halogenated aralkyloxy or phenyl, R4 is a hydroxyl-protecting group, and R5 is C1-10 alkyl which may have a substituent, comprises the steps of reacting a methyl phosphonate derivative or methyl phosphine oxide derivative with an oxyglutaric acid mono-ester to give a reaction product which comprises an oxyglutaric acid derivative having a phosphorus-containing group and a pentenedioic acid mono-ester (by-product), removing the pendenedioic acid mono-ester from the reaction product to isolate the oxyglutaric acid derivative, and converting the isolated oxyglutaric acid derivative into the oxyglutaric acid ester derivative. A process for obtaining an optically active oxyglutaric acid ester derivative is also disclosed.

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