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2-Mercapto-benzoic acid butyl ester is an organic compound with the chemical formula C11H12O2S. It is a derivative of 2-mercapto-benzoic acid, where the carboxylic acid group is esterified with butanol. 2-mercapto-benzoic acid butyl ester is characterized by the presence of a mercapto group (-SH), which provides it with unique chemical properties. It is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and as a reagent in chemical reactions. The ester is known for its potential to participate in thiol-ene reactions, which are important in polymer chemistry for creating cross-linked materials. It is also used in the preparation of certain dyes and pigments. Due to its reactivity, it is typically handled with care in a laboratory setting.

7072-70-0

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7072-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7072-70-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7072-70:
(6*7)+(5*0)+(4*7)+(3*2)+(2*7)+(1*0)=90
90 % 10 = 0
So 7072-70-0 is a valid CAS Registry Number.

7072-70-0Relevant academic research and scientific papers

Biological activity of alkyl 2-(acylthio)benzoates

Matsumura, Eiko,Nishinaka, Takahiro,Tsujibo, Hiroshi,Hachiken, Hiroko,Miki, Yasuyoshi,Sakagami, Yoshikazu,Inamori, Yoshihiko

, p. 254 - 256 (2000)

Of a series of synthetic alkyl 2-(acylthio)benzoate (1-20), all the derivatives except for n-butyl 2-butyrylthiobenzoate (18) and n-butyl 2-n- valerylthiobenzoate (20) showed clear phytogrowth-inhibitory activity. All the compounds tested except for methyl 2-butyrylthiobenzoate (3) exhibited cytotoxic activity on mouse splenic T cells. Strong phytogrowth-inhibition and cytotoxic activity were found with 1, 6, 11 and 16 with an acetylthio group at C-2, suggesting that the acetyl group seems to play an important role in both activities of alkyl 2(acylthio)benzoates. Among them, methyl 2- acetylthiobenzoate (1) was the strongest inhibitor. On the other hand, potent inhibition of prolyl endopeptidase was exhibited by 2, 7, 12 and 17 with a propionylthio group at C-2. These findings imply that a propionyl group might be useful for increasing the inhibitory activity against on prolyl endopeptidase.

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