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142038-16-2

CHEMBRDG-BB 4011074 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 142038-16-2 Structure

  • Basic information

    1. Product Name: CHEMBRDG-BB 4011074
    2. Synonyms: CHEMBRDG-BB 4011074;4-[(4-FLUOROPHENYL)THIO]BUTAN-2-ONE;4-[(4-fluorophenyl)thio]butan-2-one(SALTDATA: FREE)
    3. CAS NO:142038-16-2
    4. Molecular Formula: C10H11FOS
    5. Molecular Weight: 198.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142038-16-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 290.6°C at 760 mmHg
    3. Flash Point: 129.6°C
    4. Appearance: /
    5. Density: 1.15g/cm3
    6. Vapor Pressure: 0.00205mmHg at 25°C
    7. Refractive Index: 1.535
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: CHEMBRDG-BB 4011074(CAS DataBase Reference)
    11. NIST Chemistry Reference: CHEMBRDG-BB 4011074(142038-16-2)
    12. EPA Substance Registry System: CHEMBRDG-BB 4011074(142038-16-2)

  • Safety Data

    1. Hazard Codes: T
    2. Statements: 25
    3. Safety Statements: 45
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 142038-16-2(Hazardous Substances Data)

142038-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142038-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,0,3 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 142038-16:
(8*1)+(7*4)+(6*2)+(5*0)+(4*3)+(3*8)+(2*1)+(1*6)=92
92 % 10 = 2
So 142038-16-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H11FOS/c1-8(12)6-7-13-10-4-2-9(11)3-5-10/h2-5H,6-7H2,1H3

142038-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-fluorophenyl)sulfanylbutan-2-one

1.2 Other means of identification

Product number -
Other names 3-oxobutyl p-fluorophenyl sulfide

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:142038-16-2 SDS

142038-16-2Relevant articles and documents

Visible-Light-Mediated Alkylation of Thiophenols via Electron Donor-Acceptor Complexes Formed between Two Reactants

Cai, Yi-Ping,Nie, Fang-Yuan,Song, Qin-Hua

, p. 12419 - 12426 (2021/09/02)

A metal-free, photocatalyst-free, photochemical system was developed for the direct alkylation of thiophenols via electron donor-acceptor (EDA) complexes (KEDA = 145 M-1) between two reactants, N-hydroxyphthalimide esters as acceptors and thiophenol anions as donors, in the presence of a tertiary amine. The EDA complexes in the reaction system have a broad range of visible-light absorption (400-650 nm) and can trigger the reaction effectively under sunlight.

PYRONE COMPOUNDS AND HERBICIDES COMPRISING THE SAME

-

Paragraph 0065, (2014/05/07)

The present invention provides a compound having an excellent efficacy for controlling weeds. A pyrone compound of formula (I): wherein m is 1, 2 or 3; n is an integer of any one of 1 to 5; X represents O, S, S(O) or S(O)2; R1 repres

Remote Participation during Photooxidation at Sulfur. Eidence for Sulfurane Intermediates

Clennan, E. L.,Yang, Kang

, p. 4477 - 4487 (2007/10/02)

The photooxidations of geminally substituted γ-hydroxy sulfides results in formation of unusual oxidative elimination products.Detailed spectral data and the independent synthesis of a close analogue provide compelling evidence for the structures of these

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