Welcome to LookChem.com Sign In|Join Free
  • or
4-(p-tolylthio)benzene-1,3-diol is an organic compound with the molecular formula C13H12O2S. It is a derivative of benzene-1,3-diol, featuring a p-tolylthio group (a tolyl group attached to a sulfur atom) at the 4-position. 4-(p-tolylthio)benzene-1,3-diol is characterized by its aromatic structure, with two hydroxyl groups at the 1 and 3 positions and a sulfur atom bonded to a p-tolyl group at the 4 position. It is a colorless solid and is used in the synthesis of various organic compounds and pharmaceuticals due to its unique chemical properties. The compound is also known for its potential applications in materials science and as a precursor in the production of certain dyes and pigments.

6013-48-5

Post Buying Request

6013-48-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6013-48-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6013-48-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,1 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6013-48:
(6*6)+(5*0)+(4*1)+(3*3)+(2*4)+(1*8)=65
65 % 10 = 5
So 6013-48-5 is a valid CAS Registry Number.

6013-48-5Downstream Products

6013-48-5Relevant academic research and scientific papers

Cobalt-Catalyzed Aerobic Cross-Dehydrogenative Coupling of C-H and Thiols in Water for C-S Formation

Huang, Xin,Chen, Yongqi,Zhen, Shan,Song, Lijuan,Gao, Mingqi,Zhang, Panke,Li, Heng,Yuan, Bingxin,Yang, Guanyu

, p. 7331 - 7340 (2018)

Organosulfides have great significance and value in synthetic and biological chemistry. To establish a versatile and green methodology for C-S bond generation, we successfully developed a new aerobic cross-dehydrogenative coupling of C-H and S-H to synthe

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-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 (2016/01/09)

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.

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

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6013-48-5