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Benzene, [(2-chlorocyclopentyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 100127-09-1 Structure
  • Basic information

    1. Product Name: Benzene, [(2-chlorocyclopentyl)thio]-
    2. Synonyms:
    3. CAS NO:100127-09-1
    4. Molecular Formula: C11H13ClS
    5. Molecular Weight: 212.743
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100127-09-1.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, [(2-chlorocyclopentyl)thio]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, [(2-chlorocyclopentyl)thio]-(100127-09-1)
    11. EPA Substance Registry System: Benzene, [(2-chlorocyclopentyl)thio]-(100127-09-1)
  • 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: 100127-09-1(Hazardous Substances Data)

100127-09-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100127-09-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,2 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100127-09:
(8*1)+(7*0)+(6*0)+(5*1)+(4*2)+(3*7)+(2*0)+(1*9)=51
51 % 10 = 1
So 100127-09-1 is a valid CAS Registry Number.

100127-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-chlorocyclopentyl)sulfanylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,[(2-chlorocyclopentyl)thio]

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:100127-09-1 SDS

100127-09-1Relevant articles and documents

Regioselective Chlorothiolation of Alkenes with Sulfonyl Chlorides

Wei, Jingjing,Liang, Shuaishuai,Jiang, Lvqi,Mumtaz, Yasir,Yi, Wen-Bin

, p. 977 - 984 (2020)

Newly developed sulfonyl chloride-based regioselective chlorothiolation of alkenes has been disclosed; the reaction is compatible with a variety of functional groups and can be scaled up to the gram scale with no loss in yield. The employment of readily a

Agents for regulation of colon cancer gene expression

-

, (2008/06/13)

Compounds of the general structure according to Formula (I) wherein R1is selected from alkyl, alkenyl, alkynyl, heteroalkyl, haloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl, and heterocycloalkyl; R2is selected fro

Elimination and Addition Reactions. Part 37. A Comparative Study of Electronic, Steric , and Solvent Effects upon Reactivity in Additions of Benzenesulphenyl Chloride to Alkenes

Jones, G. Alun,Stirling, Charles J. M.,Bromby, Norman G.

, p. 385 - 394 (2007/10/02)

Rates of additions of benzenesulphenyl chloride to 35 alkenes in several solvents have been measured, and the products of the reactions have in most cases been identified.Results for arylalkenes broadly confirm previous work, but the responses to solvent change are not uniform throughout.The reactivity of bridged cycloalkanes is substantially greater than that of cycloalkenes, but that of cyclo-pentadiene dimer is anomalously small.For allylic substrates, the correlation of electron density at the double bond with reactivity is shown by a rectilinear relationship between log k and ?I.Allyl iodide and allyl alcohol are anomalously more reactive than this correlation would predict; this is accounted for by solvation and by internal solvation effects respectively.

O-SILYLATED ENOLATES IN ORGANIC SYNTHESIS: SULPHUR-MEDIATED ALKYLATION OF ESTERS WITH ALKENES.

Patel, Shailesh K.,Paterson, Ian

, p. 1315 - 1318 (2007/10/02)

O-Silylated ester enolates can be alkylated, under ZnBr2-catalysis, by the PhSCl-adducts of mono- and di-substituted alkenes to give γ-phenylthioesters, from which sulphur can be removed both reductively and oxidatively.This alkene carbosulphenylation rea

ALKENE CARBOSULPHENYLATION AND CARBOSELENYLATION: THE USE OF ALLYLTRIMETHYLSILANE AND O-SILYLATED ENOLATES.

Alexander, Rikki P.,Paterson, Ian

, p. 5911 - 5914 (2007/10/02)

Allyltrimethylsilane, as well as O-silylated enolates, can be alkylated by the PhSCl adducts of alkenes and vinyl ethers (1, X=SPh); the PhSeCl analogues (1, X=SePh), however, are less useful for alkylation purposes due to competing nucleophilic attack at selenium.

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