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143392-32-9

Benzene, 1-ethynyl-2-(phenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 143392-32-9 Structure

  • Basic information

    1. Product Name: Benzene, 1-ethynyl-2-(phenylthio)-
    2. Synonyms:
    3. CAS NO:143392-32-9
    4. Molecular Formula: C14H10S
    5. Molecular Weight: 210.299
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 143392-32-9.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: Benzene, 1-ethynyl-2-(phenylthio)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 1-ethynyl-2-(phenylthio)-(143392-32-9)
    11. EPA Substance Registry System: Benzene, 1-ethynyl-2-(phenylthio)-(143392-32-9)

  • 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: 143392-32-9(Hazardous Substances Data)

143392-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143392-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,3,9 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 143392-32:
(8*1)+(7*4)+(6*3)+(5*3)+(4*9)+(3*2)+(2*3)+(1*2)=119
119 % 10 = 9
So 143392-32-9 is a valid CAS Registry Number.

143392-32-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethynyl-2-phenylsulfanylbenzene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:143392-32-9 SDS

143392-32-9Downstream Products

143392-32-9Relevant articles and documents

Cascade Annulation of 2-Alkynylthioanisoles with Unsaturated α-Bromocarbonyls Leading to Thio-Benzobicyclic Skeletons

Gao, Yuzhen,Zhang, Pengbo,Li, Gang,Zhao, Yufen

, p. 13726 - 13733 (2018/11/30)

A protocol of Cu-catalyzed annulation of phenylethynylsulfanes with unsaturated α-bromocarbonyls for the construction of thio-benzobicyclic skeletons is described. In this single reaction, three new bonds and two new rings can be established, highlighting the step-economics and high efficiency of this protocol.

Ruthenium-catalyzed oxidative transformations of terminal alkynes to ketenes by using tethered sulfoxides: Access to β-lactams and cyclobutanones

Wang, Youliang,Zheng, Zhitong,Zhang, Liming

, p. 9572 - 9576 (2014/10/15)

The oxidation of in situ generated Ru vinylidenes to ketenes is realized with tethered sulfoxides. The result is a Ru-catalyzed oxidative transformation of terminal alkynes to highly valuable ketenes. Moreover, the ketenes generated here were shown to und

Base-Induced Selective Ring Opening of 1-Arylbenzothiophenium Salts

Kitamura, Tsugio,Takachi, Tatsuya,Soda, Shin-ichi,Kawasato, Hironobu,Taniguchi, Hiroshi

, p. 1357 - 1360 (2007/10/02)

Reactions of 1-arylbenzothiophenium salts with methoxide anion in methanol caused the fission of the S+-C(2) bond of the thiophenium ring to produce o-(phenylthio)phenyl-substituted methoxyethenes, allenes, or alkynes.

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