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2-<3-<3-(5-t-butyl-2-hydroxyphenylthio)-5-t-butyl-2-hydroxyphenylthio>-5-t-butylsalicyl>-4-t-butylphenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133785-87-2

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133785-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133785-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,7,8 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133785-87:
(8*1)+(7*3)+(6*3)+(5*7)+(4*8)+(3*5)+(2*8)+(1*7)=152
152 % 10 = 2
So 133785-87-2 is a valid CAS Registry Number.

133785-87-2Downstream Products

133785-87-2Relevant academic research and scientific papers

A new synthesis of allyl ethers via allyldialkyltelluronium salts

Xu,Lu,Huang

, p. 2527 - 2531 (1993)

Allyldialkyltelluronium bromides were treated with phenols in the presence of NaOH at room temperature, readily giving allyl aromatic ethers in excellent yields. This procedure represents an efficient means for synthesis of allyl aromatic ethers.

Synthesis and Inclusion Properties of Sulfur-Bridged Analogs of Acyclic Phenol-Formaldehyde Oligomers

Ohba, Yoshihiro,Moriya, Kazuhiko,Sone, Tyo

, p. 576 - 582 (2007/10/02)

A series of compounds in which a part or all of the methylene bridges of acyclic p-methyl- and p-t-butylphenol-formaldehyde tetramers were replaced by sulfur bridge(s) was synthesized.It was found that though the sulfur-bridged tetramers formed crystalline host-guest complexes with a variety of organic compounds, they were different from the parent tetramers regarding their inclusion behavior.The number and position of the sulfur bridge(s), as well as the p-substituent of phenol in the tetramers, had a great influence upon the inclusion property.The thermal stability of complexes of the sulfur-bridged tetramers (SSS-a,b) with benzene, as estimated from their thermal dissociation rates, are lower than those of the parent tetramers (CCC-a,b).

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