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1522-89-0

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1522-89-0 Usage

Structure

2,2-bis(tosyloxymethyl)propane-1,3-diyl bis(4-methylbenzenesulfonate) is derived from propane and contains two tosylate groups.

Functional groups

Tosylate, benzene, and sulfonate groups.

Physical properties

Not provided in the material.

Chemical properties

Reacts with other molecules to form strong covalent bonds, which can modify the physical and chemical properties of the resulting material.

Uses

It is used as a cross-linking agent in the synthesis of polymers and resins, commonly used in the production of thermosetting plastics, adhesives, coatings, and in the modification of natural polymers to enhance their performance.

Safety precautions

It is toxic and can cause irritation to the skin and respiratory system, so it should be handled with care.

Check Digit Verification of cas no

The CAS Registry Mumber 1522-89-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1522-89:
(6*1)+(5*5)+(4*2)+(3*2)+(2*8)+(1*9)=70
70 % 10 = 0
So 1522-89-0 is a valid CAS Registry Number.
InChI:InChI=1/C33H36O12S4/c1-25-5-13-29(14-6-25)46(34,35)42-21-33(22-43-47(36,37)30-15-7-26(2)8-16-30,23-44-48(38,39)31-17-9-27(3)10-18-31)24-45-49(40,41)32-19-11-28(4)12-20-32/h5-20H,21-24H2,1-4H3

1522-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(4-methylphenyl)sulfonyloxy-2,2-bis[(4-methylphenyl)sulfonyloxymethyl]propyl] 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names 1,1,1,1-tetrakis-(tosyloxymethyl)metane

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:1522-89-0 SDS

1522-89-0Relevant articles and documents

Precisely tunable engineering of sub-30 nm monodisperse oligonucleotide nanoparticles

Sizovs, Antons,Song, Xianzhou,Waxham, M. Neal,Jia, Yilong,Feng, Fude,Chen, Jianwei,Wicker, Amanda C.,Xu, Jianming,Yu, Yan,Wang, Jin

, p. 234 - 240 (2014)

Advancement of RNAi therapies is mainly hindered by the development of efficient delivery vehicles. The ability to create small size (30 nm) oligonucleotide nanoparticles is essential for many aspects of the delivery process but is often overlooked. In t

Synthesis and antibacterial activity of new tetrakisquaternary ammonium compounds based on pentaerythritol and 3-hydroxypyridine

Vereshchagin,Minaeva,Egorov

, p. 545 - 548 (2021)

Tetrakisquaternary ammonium compounds based on pentaerythritol were synthesized for the first time. Bacteriostatic effect of the obtained compounds was evaluated towards opportunistic gram-positive Methicillin-resistant Staphylococcus aureus (strain ATCC

(S) or (R)-diphenyl-pyrrolidine methanol immobilized by pentaerythritol and its preparation method and application

-

Paragraph 0012, (2018/03/28)

The invention discloses a (S/R)-diphenyl-pyrrolidine methanol immobilized by pentaerythritol and its preparation method and application. The (S/R)-diphenyl-pyrrolidine methanol is shown as Formula (I). The preparation of the catalyst includes steps of reacting pentaerythritol with paratoluensulfonyl chloride to obtain pentaerythritol sulphonate; reacting with sodium azide to obtain pentaerythritecompound; reacting (S/R)-N-Cbz-4-hydroxyproline methyl ester with propargyl bromide to obtain (S/R)-N-Cbz-4-acetylene methoxy proline methyl ester; then reacting with chlorophenylmagnesium to obtain (S/R)-diphenyl-pyrrolidine methanol immobilized by pentaerythritol. The (S/R)-diphenyl-pyrrolidine methanol immobilized by pentaerythritol can be applied to the reaction of asymmetrical transformationand generation of prochiral phenyl ketones to be (R/S)- secondary alcohol; the catalyst can be recycled.

Four (4-triazole phenyl) qtr fifth heavenly stem four ether preparation method and application

-

Paragraph 0031, (2017/03/14)

A tetra(4-triazolephenyl) pentaerythritol ether single crystal and a preparing method thereof are disclosed. The tetra(4-triazolephenyl) pentaerythritol ether single crystal is prepared by adopting a "one-pot" method, namely by heating p-bromophenyl penta

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