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124213-39-4

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124213-39-4 Usage

Molecular structure

The compound has a complex molecular structure that includes an ethyl 4-methylbenzenesulfonate group, as well as allyloxy and p-tolylsulfonyloxy groups.

Sulfonate ester

The compound is a sulfonate ester, which is a type of organic compound that contains a sulfur-oxygen bond and an ester functional group.

Reagent in organic synthesis

The compound is commonly used as a reagent in organic synthesis and chemical reactions.

Protecting group

The compound is often used as a protecting group in organic chemistry, which temporarily blocks the reactivity of certain functional groups while allowing other reactions to occur.

Versatile compound

The presence of the allyloxy and p-tolylsulfonyloxy groups makes the compound versatile for use in a variety of chemical reactions and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 124213-39-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,2,1 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124213-39:
(8*1)+(7*2)+(6*4)+(5*2)+(4*1)+(3*3)+(2*3)+(1*9)=84
84 % 10 = 4
So 124213-39-4 is a valid CAS Registry Number.

124213-39-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Allyloxymethyl-3-oxapentanediol-1,5-ditosylate

1.2 Other means of identification

Product number -
Other names -

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:124213-39-4 SDS

124213-39-4Relevant articles and documents

Synthesis of New Alkyl- Alkenyloxy- and Hydroxy-substituted Diaza-crown Compounds

Bradshaw, Jerald S.,Krakowiak, Krzysztof E.,Izatt, Reed M.

, p. 565 - 569 (2007/10/02)

New diaza-crown compounds with the macro ring nitrogen atoms situated in the 1,4-, 1,7- and 1,10-positions have been prepared.All of the new macrocycles contain alkyl groups on the nitrogen atoms and a functional group substituent in the form of either an

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