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The chemical compound "2-<3-(3-chloromethyl-5-tert-butylsalicyl)-5-tert-butylsalicyl>-6-chloromethyl-4-tert-butylphenol" is a complex organic molecule with a molecular formula of C31H40Cl2O2. It is characterized by a phenol core with multiple chloromethyl and tert-butyl substituents. The compound features a 2-phenol group, with a 3-(3-chloromethyl-5-tert-butylsalicyl)-5-tert-butylsalicyl group attached at the 2-position and a 6-chloromethyl group at the 6-position. This molecule is likely to be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its complex structure and potential reactivity. Its specific applications and properties would depend on the context in which it is used, and further research would be required to understand its full potential and behavior in various chemical reactions.

2422-83-5

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2422-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2422-83-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2422-83:
(6*2)+(5*4)+(4*2)+(3*2)+(2*8)+(1*3)=65
65 % 10 = 5
So 2422-83-5 is a valid CAS Registry Number.

2422-83-5Downstream Products

2422-83-5Relevant academic research and scientific papers

Syntheses and properties of chiral pentahomothiazacalix[3]arenes

Ito, Kazuaki,Ohba, Yoshihiro,Sone, Tyo

, p. 1317 - 1323 (1998)

Chiral calixarene analogs incorporating an aminoethanethiol unit such as L-cysteine into their rings were prepared. Conformational analysis of the macrocycles by using 1H and 13C nmr spectroscopy revealed that their preferred conform

Synthesis and properties of pentahomothiazacalix[3]arene derivatives constructed from phenol-formaldehyde trimer and aminoethanethiol unit

Ito, Kazuaki,Ohba, Yoshihiro,Sone, Tyo

, p. 183 - 184 (1996)

Chiral calixarene analogs incorporating aminoethanethiol unit such as L-cysteine alkyl ester into their rings were prepared. NMR studies of the macrocycles reveal that their preferred conformations in solution are a cone form and the introduction of amino

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