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CAS

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131866-23-4

(5-CHLORO-3-METHYL-1-BENZOFURAN-2-YL)(4-CHLOROPHENYL)METHANONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131866-23-4 Structure

  • Basic information

    1. Product Name: (5-CHLORO-3-METHYL-1-BENZOFURAN-2-YL)(4-CHLOROPHENYL)METHANONE
    2. Synonyms: (5-CHLORO-3-METHYL-1-BENZOFURAN-2-YL)(4-CHLOROPHENYL)METHANONE
    3. CAS NO:131866-23-4
    4. Molecular Formula: C16H10Cl2O2
    5. Molecular Weight: 305.16
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131866-23-4.mol

  • Chemical Properties

    1. Melting Point: 123 °C(Solv: ethanol (64-17-5))
    2. Boiling Point: 419.5±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.358±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (5-CHLORO-3-METHYL-1-BENZOFURAN-2-YL)(4-CHLOROPHENYL)METHANONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5-CHLORO-3-METHYL-1-BENZOFURAN-2-YL)(4-CHLOROPHENYL)METHANONE(131866-23-4)
    11. EPA Substance Registry System: (5-CHLORO-3-METHYL-1-BENZOFURAN-2-YL)(4-CHLOROPHENYL)METHANONE(131866-23-4)

  • 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: 131866-23-4(Hazardous Substances Data)

131866-23-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131866-23-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,8,6 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 131866-23:
(8*1)+(7*3)+(6*1)+(5*8)+(4*6)+(3*6)+(2*2)+(1*3)=124
124 % 10 = 4
So 131866-23-4 is a valid CAS Registry Number.

131866-23-4Relevant articles and documents

Solution-phase photochemical transformation of 2-aroylbenzofurans: Addition-elimination mechanism

Jindal, Pooja,Sharma, Geeta,Arora, Rita,Kamboj, Ramesh C.

, p. 4465 - 4476 (2015/06/30)

An efficient conversion of 2-aroylbenzofurans into arylbenzofurylmethanols through photoreduction has been described. In these molecules, the photo transformation occurred through the initial addition of solvent followed by elimination involving γ-hydroge

Synthesis and?antifungal activities of?some?aryl [3-(imidazol-1-yl/triazol-1-ylmethyl) benzofuran-2-yl] ketoximes

Gündo?du-Karaburun, Nalan,Benkli, Kadriye,Tunali, Ya?mur,U?ucu, ümit,Demirayak, ?eref

, p. 651 - 656 (2007/10/03)

In this study, some aryl [3-(imidazol-1-yl/triazol-1-ylmethyl)benzofuran-2-yl] ketones, aryl (3-methyl-benzofuran-2-yl) ketoximes and aryl [3-(imidazol-1-yl/triazol-1-ylmethyl)benzofuran-2-yl] ketoximes were synthesised starting from 2-aryloyl-3-methyl-be

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