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1394124-47-0

S-(2-fluorophenyl) benzenesulfonothioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1394124-47-0 Structure

  • Basic information

    1. Product Name: S-(2-fluorophenyl) benzenesulfonothioate
    2. Synonyms: S-(2-fluorophenyl) benzenesulfonothioate
    3. CAS NO:1394124-47-0
    4. Molecular Formula:
    5. Molecular Weight: 268.333
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1394124-47-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: S-(2-fluorophenyl) benzenesulfonothioate(CAS DataBase Reference)
    10. NIST Chemistry Reference: S-(2-fluorophenyl) benzenesulfonothioate(1394124-47-0)
    11. EPA Substance Registry System: S-(2-fluorophenyl) benzenesulfonothioate(1394124-47-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1394124-47-0(Hazardous Substances Data)

1394124-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1394124-47-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,1,2 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1394124-47:
(9*1)+(8*3)+(7*9)+(6*4)+(5*1)+(4*2)+(3*4)+(2*4)+(1*7)=160
160 % 10 = 0
So 1394124-47-0 is a valid CAS Registry Number.

1394124-47-0Downstream Products

1394124-47-0Relevant articles and documents

Visible-light-promoted synthesis of secondary and tertiary thiocarbamates from thiosulfonates andN-substituted formamides

Bi, Wen-Zhu,Zhang, Wen-Jie,Li, Zi-Jie,He, Yuan-Hao,Feng, Su-Xiang,Geng, Yang,Chen, Xiao-Lan,Qu, Ling-Bo

supporting information, p. 8701 - 8705 (2021/10/22)

A general visible-light-promoted metal-free synthesis of secondary and tertiary thiocarbamates starting from thiosulfonates andN-substituted formamides is developed. By employing rhodamine B as a photocatalyst andtert-butyl hydroperoxide (TBHP) as an oxidant, a wide scope of thiocarbamates can be obtained through direct thiolation of acyl C-H bonds under irradiation of blue light at room temperature for 12 h.

Visible-light induced decarboxylative coupling of redox-active esters with disulfides to construct C-S bonds

Xiao, Zhiwei,Wang, Lu,Wei, Junjie,Ran, Chongzhao,Liang, Steven H.,Shang, Jingjie,Chen, Guang-Ying,Zheng, Chao

supporting information, p. 4164 - 4167 (2020/04/22)

A novel method has been established for the construction of C-S bonds using redox-active esters with disulfides in the presence of Ru-photoredox catalyst. This method exhibits remarkable functional group tolerance across a wide scope of substrates. Under

Metal-free NaI/TBHP-mediated sulfonylation of thiols with sulfonyl hydrazides

Chen, Qian,Huang, Yulin,Wang, Xiaofeng,Wu, Jiawei,Yu, Guodian

, p. 1713 - 1719 (2018/03/21)

A highly efficient sulfonylation of thiols has been achieved through the metal-free NaI/TBHP-mediated cross-coupling of sulfonyl hydrazides and thiols at room temperature. This method provides a convenient and practical route to thiosulfonates in 84-99% y

NBS-promoted sulfenylation of sulfinates with disulfides leading to unsymmetrical or symmetrical thiosulfonates

Liang, Gaigai,Liu, Miaochang,Chen, Jiuxi,Ding, Jinchang,Gao, Wenxia,Wu, Huayue

experimental part, p. 1611 - 1616 (2012/09/07)

A highly practical method to access unsymmetrical and symmetrical thiosulfonates in moderate to excellent yields has been developed through NBS-promoted sulfenylation of sulfinates with disulfides. The present process enables the use of two RS in RSSR and shows broad functional group tolerance, which represents an atom-economical and practical procedure for the synthesis of thiosulfonates. A plausible mechanism for the role of NBS as a promoter for the cleavage of disulfides generating N-(organothio)succinimide that then undergos facile sulenylation with sulfinates is proposed. Copyright

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