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CAS

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172933-33-4

5-chloro-2-[(4,4-difluorobut-3-en-1-yl)sulfonyl]-1,3-thiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 172933-33-4 Structure

  • Basic information

    1. Product Name: 5-chloro-2-[(4,4-difluorobut-3-en-1-yl)sulfonyl]-1,3-thiazole
    2. Synonyms: thiazole, 5-chloro-2-[(4,4-difluoro-3-buten-1-yl)sulfonyl]-
    3. CAS NO:172933-33-4
    4. Molecular Formula: C7H6ClF2NO2S2
    5. Molecular Weight: 273.7078
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 172933-33-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 356.503°C at 760 mmHg
    3. Flash Point: 169.407°C
    4. Appearance: N/A
    5. Density: 1.523g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.522
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-chloro-2-[(4,4-difluorobut-3-en-1-yl)sulfonyl]-1,3-thiazole(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-chloro-2-[(4,4-difluorobut-3-en-1-yl)sulfonyl]-1,3-thiazole(172933-33-4)
    12. EPA Substance Registry System: 5-chloro-2-[(4,4-difluorobut-3-en-1-yl)sulfonyl]-1,3-thiazole(172933-33-4)

  • 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: 172933-33-4(Hazardous Substances Data)

172933-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 172933-33-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,9,3 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 172933-33:
(8*1)+(7*7)+(6*2)+(5*9)+(4*3)+(3*3)+(2*3)+(1*3)=144
144 % 10 = 4
So 172933-33-4 is a valid CAS Registry Number.

172933-33-4Downstream Products

172933-33-4Relevant articles and documents

Processes for the production of 5-chloro-2-(4,4-difluorobut-3-enylsulphonyl)thiazole

-

, (2008/06/13)

5-Chloro-2-(4,4-difluorobutenylthio)thiazole is prepared from 2-mercaptothiazole by a multistep process involving S-alkylation, chlorination and dehydrochlorination and is converted by oxidation to the corresponding sulfone which is useful as an agricultural nematicide.

Oxazoles and their agricultural compositions

-

, (2008/06/13)

A compound having the formula R--S(O)n CH2 CH2 CH=CF2, wherein R is a phenyl group or a heterocyclic group selected from furyl, thienyl, isoxazolyl, isothiazolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, 1,2,4-oxadiazolyl, 1,2,4-thiadiazolyl, 1,3,4-oxadiazolyl, 1,3,4-thidiazolyl, tetrazolyl, pyridyl, pyridazinyl, pyrazinyl, 1,2,3-triazinyl, 1,3,4-triazinyl, and 1,3,5-triazinyl groups, said phenyl or heterocyclic group being optionally substituted by optionally substituted alkyl, optionally substituted alkenyl, alkynyl, cycloalkyl, alkylcycloalkyl, alkoxy, alkenyloxy, alkynyloxy, hydroxyalkyl, alkoxyalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, optionally substituted aryloxy, optionally substituted arylalkoxy, optionally substituted aryloxyalkyl, optionally substituted heteroaryloxy, optionally substituted heteroarylalkoxy, optionally substituted heteroaryloxyalkyl, haloalkyl, haloalkenyl, haloalkynyl, haloalkoxy, haloalkenyloxy, haloalkynyloxy, halogen, hydroxy, cyano, nitro, --NR7R8, --NR7COR8, --NR7CSR8, --NR7SO2R8, --N(SO2R7)(SO2R8), --COR7, --CONR7R8, -alkylCONR7R8, --CR7NR8, --COOR7, --OCOR7, --SR7, --SOR7, --SO2R7, -alkylSR7, -alkylSOR7, -alkylSO2R7, --OSO2R7, --SO2NR7R8, --CSNR7R8, --SiR7R8R9, --OCH2CO2R7, --OCH2CH2CO2R7, --CONR7SO2R8, -alkylCONR7SO2R8, --NHCONR7R8, --NHCSNR7R8, or an adjacent pair of R1, R2, R3, R4, R5 and R6 when taken together form a fused 5- or 6-membered carbocyclic or heterocyclic ring; R7, R8 and R9 are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, alkynyl, optionally substituted aryl or optionally substituted arylalkyl, haloalkyl, haloalkenyl, haloalkynyl, halogen or hydroxy.

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