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4-(phenylthio)benzene-1,3-diol, also known as 4-phenylthioresorcinol or 4-(phenylthio)resorcinol, is an organic compound with the chemical formula C12H10O2S. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. 4-(phenylthio)benzene-1,3-diol is characterized by a benzene ring with two hydroxyl groups at the 1 and 3 positions and a phenylthio group attached at the 4 position. It is used as a reagent in various analytical applications, particularly in the determination of metal ions such as iron, copper, and zinc, due to its ability to form colored complexes with these ions. The compound is also of interest in the synthesis of other organic compounds and in the study of chemical reactions involving phenylthio groups.

5633-58-9

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5633-58-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5633-58-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5633-58:
(6*5)+(5*6)+(4*3)+(3*3)+(2*5)+(1*8)=99
99 % 10 = 9
So 5633-58-9 is a valid CAS Registry Number.

5633-58-9Downstream Products

5633-58-9Relevant academic research and scientific papers

Iodine-mediated thiolation of phenol/phenylamine derivatives and sodium arylsulfinates in neat water

Wang, Dingyi,Zhang, Rongxing,Lin, Sen,Yan, Zhaohua,Guo, Shengmei

, p. 108030 - 108033 (2015)

An efficient and convenient protocol for iodine-mediated thiolation of phenols/phenylamines with sodium benzene-sulfinates in water has been achieved. In this transformation, environment-friendly conditions (including metal-free and water as solvent) are employed under air conditions, and a series of valuable thioethers are easily obtained in moderate to good yields.

TBAI-HBr system mediated generation of various thioethers with benzenesulfonyl chlorides in PEG400

Wang, Dingyi,Guo, Shengmei,Zhang, Rongxing,Lin, Sen,Yan, Zhaohua

, p. 54377 - 54381 (2016/07/06)

An efficient procedure for the formation of C-S bonds via C-H functionalization was developed for the synthesis of aryl sulfides in good to excellent yields using TBAI-HBr system promoted direct sulfenylation of various compounds, such as phenols, pyrazolones, indoles and related heteroarenes. Low cost and widely available arylsulfonyl chlorides were used as the sulfur source to provide various sulfur-containing compounds. The characteristic of the present protocol is convenient, green, highly efficient with a wide-application and short reaction time.

Iodine catalyzed cross-dehydrogenative C-S coupling by C(sp2)-H bond activation: Direct access to aryl sulfides from aryl thiols

Parumala, Santosh Kumar Reddy,Peddinti, Rama Krishna

supporting information, p. 4068 - 4072 (2015/07/15)

A novel, efficient and unprecedented green protocol for the formation of C-S bonds has been developed under metal-free conditions. This protocol involves the synthesis of aryl sulfides through the cross-dehydrogenative coupling of readily available aryl t

Topical process for lightening the skin or treating pigmental blemishes using a composition containing 4-thioresorcin derivatives

-

, (2008/06/13)

A topical process for lightening the skin or treating pigmental blemishes consisting in applying to the part of the skin to be treated a composition containing, as active compounds, 4-thioresorcin derivatives corresponding to the following formula: STR1 w

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