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2-Mercapto-4,6-di-tert-butylphenol, with the CAS number 53551-74-9, is a light yellow solid compound that is primarily utilized in the field of organic synthesis. It is known for its unique chemical properties that make it a valuable component in various chemical reactions and processes.

53551-74-9

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53551-74-9 Usage

Uses

Used in Organic Synthesis:
2-Mercapto-4,6-di-tert-butylphenol is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and reactivity allow it to participate in a wide range of chemical reactions, making it a versatile building block for the creation of new molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Mercapto-4,6-di-tert-butylphenol is used as a starting material for the development of new drugs. Its chemical properties enable it to be modified and functionalized to create novel drug candidates with potential therapeutic benefits.
Used in Chemical Research:
2-Mercapto-4,6-di-tert-butylphenol is also employed in chemical research as a model compound for studying various reaction mechanisms and exploring new synthetic routes. Its unique properties make it an ideal candidate for investigating the reactivity of similar compounds and understanding the underlying principles governing their behavior.
Used in Material Science:
In the field of material science, 2-Mercapto-4,6-di-tert-butylphenol can be used as a component in the development of new materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of novel materials with enhanced characteristics, such as improved stability, reactivity, or selectivity.
Overall, 2-Mercapto-4,6-di-tert-butylphenol is a versatile compound with a wide range of applications across various industries, including organic synthesis, pharmaceuticals, chemical research, and material science. Its unique chemical properties and reactivity make it a valuable asset in the development of new compounds, materials, and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 53551-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,5 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53551-74:
(7*5)+(6*3)+(5*5)+(4*5)+(3*1)+(2*7)+(1*4)=119
119 % 10 = 9
So 53551-74-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H22OS/c1-13(2,3)9-7-10(14(4,5)6)12(15)11(16)8-9/h7-8,15-16H,1-6H3

53551-74-9SDS

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 2,4-ditert-butyl-6-sulfanylphenol

1.2 Other means of identification

Product number -
Other names 4,6-Di-tert-butyl-2-mercaptophenol

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:53551-74-9 SDS

53551-74-9Relevant academic research and scientific papers

Syndiospecific polymerization of styrene with C1-symmetric [OSNO]-type bridged bis(phenolate) titanium (IV) complexes

Zhou, QiHua,Liang, HuaQing,Long, YongJiang,Wu, Qing,Gao, HaiYang,Liang, GuoDong,Zhu, FangMing

, p. 347 - 353 (2015/12/18)

Two C1-symmetric [OSNO]-type ethanediyl-bridged imine-thiobis(phenolate) titanium (IV) complexes of [Ti(OC6H2-6-tBu-4-tBu)2{CH=N(CH2)2SCH2}Cl2] a

Electronic and hydrogen bonding effects on the chain-breaking activity of sulfur-containing phenolic antioxidants

Amorati, Riccardo,Fumo, Maria Grazia,Menichetti, Stefano,Mugnaini, Veronica,Pedulli, Gian Franco

, p. 6325 - 6332 (2007/10/03)

A kinetic and thermodynamic investigation of phenols para-substituted with thiyl (SR), sulfinyl (SOR), and sulfonyl (SO2R) groups and ortho-substituted with thiyl groups is reported. The effect of the sulfur substituents on the O-H bond dissoci

Dibenzodioxadithiasilonin: Synthesis and Characterization

Pastor, Stephen D.,Denney, Dorothy Z.

, p. 681 - 683 (2007/10/02)

The reaction of 2,4-di-t-butylphenol, 4, with sulfur monochloride gave the trithiobisphenol 5 rather than the expected dithiobisphenol 7.The thiol 6 was obtained by the reduction of 5 with zinc under acidic conditions.The dithiobisphenol 7 was prepared by

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