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1,2-Ethanediol, 1-(4-chloro-2,3-dihydro-1,1-dioxido-3-thienyl)-, 2-benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 142776-01-0 Structure
  • Basic information

    1. Product Name: 1,2-Ethanediol, 1-(4-chloro-2,3-dihydro-1,1-dioxido-3-thienyl)-, 2-benzoate
    2. Synonyms:
    3. CAS NO:142776-01-0
    4. Molecular Formula: C13H13ClO5S
    5. Molecular Weight: 316.762
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142776-01-0.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: 1,2-Ethanediol, 1-(4-chloro-2,3-dihydro-1,1-dioxido-3-thienyl)-, 2-benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Ethanediol, 1-(4-chloro-2,3-dihydro-1,1-dioxido-3-thienyl)-, 2-benzoate(142776-01-0)
    11. EPA Substance Registry System: 1,2-Ethanediol, 1-(4-chloro-2,3-dihydro-1,1-dioxido-3-thienyl)-, 2-benzoate(142776-01-0)
  • 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: 142776-01-0(Hazardous Substances Data)

142776-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142776-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,7 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 142776-01:
(8*1)+(7*4)+(6*2)+(5*7)+(4*7)+(3*6)+(2*0)+(1*1)=130
130 % 10 = 0
So 142776-01-0 is a valid CAS Registry Number.

142776-01-0Relevant articles and documents

A Cyclization Approach toward Five-Membered Heteroaromatic o-Quinodimethanes via Fused-3-Sulfolenes

Chou, Ta-Shue,Tsai, Chung-Ying,Lee, Shwu-Jiuan

, p. 299 - 307 (2007/10/03)

A general strategy involving the zincation of 4-bromo-3-chloro-2-sulfolene, in situ condensation with an α-heterosubstituted acetaldehyde, and subsequent cyclization reaction as the key steps toward the synthesis of furano- and thieno-3-sulfolenes is desc

SYNTHESIS OF FURAN-FUSED 3-SULFOLENE. A STABLE PRECURSOR TO FURAN ANALOGUE OF o-QUINODIMETHANE

Chou, Ta-shue,Tsai, Chung-Ying

, p. 663 - 666 (2007/10/02)

Ultrasound-promoted zincation of 2-chloro-4-bromo-2-sulfolene (10) with benzoyloxyacetaldehyde (6), followed by base-induced hydrolysis, intramolecular conjugate addition and aromatization, gives the 3-sulfolene (4) which is a stable precursor to the fura

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