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4-Hydroxybutyl 4-methylbenzenesulfonate is a chemical compound with the molecular formula C11H14O4S. It is an ester derivative of 4-methylbenzenesulfonic acid, where the hydroxybutyl group is attached to the benzene ring. 4-hydroxybutyl 4-methylbenzenesulfonate is characterized by its ability to form esters with alcohols and is often used in organic synthesis, particularly in the preparation of pharmaceuticals and other specialty chemicals. It is known for its solubility in organic solvents and its potential applications in the chemical industry. The compound's structure features a hydroxybutyl chain that provides it with unique reactivity and properties, making it a valuable intermediate in the synthesis of various compounds.

6972-09-4

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6972-09-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6972-09-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6972-09:
(6*6)+(5*9)+(4*7)+(3*2)+(2*0)+(1*9)=124
124 % 10 = 4
So 6972-09-4 is a valid CAS Registry Number.

6972-09-4SDS

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 4-hydroxybutyl 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names Toluene-4-sulfonic acid 4-hydroxy-butyl 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:6972-09-4 SDS

6972-09-4Relevant academic research and scientific papers

HETEROBIFUNCTIONAL MOLECULES AS TEAD INHIBITORS

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Paragraph 0259-0260, (2021/09/11)

The invention relates to compounds and methods of using said compounds, as well as pharmaceutical compositions containing such compounds, for treating diseases and conditions mediated by TEAD, such as cancer.

Rapid synthesis of the core scaffold of crinane and haemanthamine through a multi-component approach

Massaro, Nicholas P.,Pierce, Joshua G.

supporting information, (2021/06/09)

A rapid synthesis of the core structures of crinane and haemanthamine has been developed, enabled by a multicomponent approach. This work constitutes a formal synthesis of crinane and sets the stage for access to both families of natural products and key

NOVEL COMPOUND For Organic light emitting diode AND COATING COMPOSITION FOR ORGANIC LAYER COMPRISING THE SAME

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Paragraph 0137; 0138; 0139; 0140; 0175; 0176; 0177; 0178, (2020/12/29)

Provided are a compound represented by chemical formula (1) and a coating liquid composition comprising the same. The above formula (1) is as described in the description of the invention.

IRAK DEGRADERS AND USES THEREOF

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Paragraph 00962; 004961-004962, (2020/06/19)

The present invention provides compounds, compositions thereof, and methods of using the same.

Stereoselective, Multicomponent Approach to Quaternary Substituted Hydroindole Scaffolds

Massaro, Nicholas P.,Pierce, Joshua G.

supporting information, p. 5079 - 5084 (2020/07/04)

The Amaryllidaceae alkaloids have been a target of synthesis for decades due to their complex architectures and biological activity. A central feature of these natural product cores is a quaternary substituted hydroindole heterocycle. Building off the fou

A 4 - mercapto -1 - butanol synthesis process

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Paragraph 0032; 0033; 0034, (2017/05/02)

The present invention discloses a 4-mercapto-1-butanol synthesis process, which comprises: 1) dissolving 1,4-butanediol and an acid-binding agent in an organic solvent I, adding a sulfonylation agent in a dropwise manner to carry out a sulfonylation reaction, carrying out extraction separation with dichloromethane, and carrying out washing, drying and concentration to obtain a colorless oil-like substance; and 2) dissolving the colorless oil-like substance obtained in the step 1) in an organic solvent II, adding a nucleophile to carry out a nucleophilic substitution reaction, and finally carrying out pressure reducing distillation to obtain the 4-mercapto-1-butanol. According to the present invention, the completely-new 4-mercapto-1-butanol synthesis route is provided, the used raw materials are easy to obtain, the operation is simple, the reaction conditions are not harsh, and good industrial values are provided.

Quinazoline Derivatives Useful as CB-1 Inverse Agonists

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Paragraph 0536-0537, (2016/04/20)

The present invention is directed to quinazoline derivatives, pharmaceutical compositions containing said derivatives and their use in the treatment of disorders and conditions mediated by the CB-1 receptor; more particularly, in the treatment of disorders and conditions responsive to inverse agonism of the CB-1 receptor. For example, the compounds of the present invention are useful in the treatment of metabolic disorders.

Novel compound capable of activating Nrf2, and pharmaceutical compositions comprising the same

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Paragraph 0077-0079, (2016/10/08)

The present invention provides a novel compound which can activate Nrf2 that is a transcription factor for expression of the quinone reductase gene. Therefore the compound is effective for inhibiting apoptosis and preventing and treating brain nerve disea

A practical and scalable process to selectively monofunctionalize water-soluble α,ω-diols

Zhang, Quanxuan,Ren, Hong,Baker, Gregory L.

supporting information, p. 3384 - 3386 (2014/06/09)

A practical protocol for rapid and scalable synthesis of monofunctionalized α,ω-diols using a simple and inexpensive THP ether protection/deprotection strategy was described. Use of inexpensive DHP source and ease to remove excess water-soluble α,ω-diols

RADIOHALOTHYMIDINES AND METHODS OF THEIR SYNTHESIS AND USE IN PET IMAGING OF CANCERS

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Page/Page column 18, (2008/06/13)

We disclose methods of synthesizing radiohalidated organic compounds and their use in positron emission tomography (PET) imaging of cancer cells. We also disclose specific N3 -radiohaloalkyl thymidines and salts thereof.

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