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120007-64-9

2-(1,3-benzoxazol-2-ylsulfanyl)-1-(4-chlorophenyl)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 120007-64-9 Structure

  • Basic information

    1. Product Name: 2-(1,3-benzoxazol-2-ylsulfanyl)-1-(4-chlorophenyl)ethanone
    2. Synonyms: 2-(1,3-benzoxazol-2-ylsulfanyl)-1-(4-chlorophenyl)ethanone
    3. CAS NO:120007-64-9
    4. Molecular Formula: C15H10ClNO2S
    5. Molecular Weight: 303.7634
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 120007-64-9.mol

  • Chemical Properties

    1. Melting Point: 129-130 °C(Solv: ligroine (8032-32-4))
    2. Boiling Point: 476.8±51.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.41±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 0.74±0.10(Predicted)
    10. CAS DataBase Reference: 2-(1,3-benzoxazol-2-ylsulfanyl)-1-(4-chlorophenyl)ethanone(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(1,3-benzoxazol-2-ylsulfanyl)-1-(4-chlorophenyl)ethanone(120007-64-9)
    12. EPA Substance Registry System: 2-(1,3-benzoxazol-2-ylsulfanyl)-1-(4-chlorophenyl)ethanone(120007-64-9)

  • 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: 120007-64-9(Hazardous Substances Data)

120007-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120007-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,0,0 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 120007-64:
(8*1)+(7*2)+(6*0)+(5*0)+(4*0)+(3*7)+(2*6)+(1*4)=59
59 % 10 = 9
So 120007-64-9 is a valid CAS Registry Number.

120007-64-9Relevant articles and documents

In vitro anti-Candida activity and action mode of benzoxazole derivatives

?ukowska-Chojnacka, Edyta,Baran, Joanna,Gryciuk, Aleksander,Kawalec, Joanna,Kowalkowska, Anna,Kuryk, ?ukasz,Rogalska, Marta,Staniszewska, Monika

, (2021/08/30)

A newly synthetized series of N-phenacyl derivatives of 2-mercaptobenzoxazole, including analogues of 5-bromo- and 5,7-dibromobenzoxazole, were screened against Candida strains and the action mechanism was evaluated. 2-(1,3-benzoxazol-2-ylsulfanyl)-1-(4-b

Synthesis of difluorinated β-ketosulfones and novel gem-difluoromethylsulfone-containing heterocycles as fluorinated building blocks

Loghmani-Khouzani, Hossein,Hajiheidari, Dariush

experimental part, p. 561 - 569 (2010/05/18)

A series of new heterocyclic β-ketosulfides was prepared by the reaction of the corresponding heterocyclic thiols with α-bromoacetophenone and its derivatives. Oxidation of the products using m-CPBA gave the corresponding heterocyclic β-ketosulfones, whic

BENZOXAZOLINONES. VI. REACTION OF BENZOXAZOLINONE AND OF BENZOAZOLINETHIONE WITH SUBSTITUTED α-HALO CARBONYL COMPOUNDS

Aflyatunova, R. G.,Babakhanova, Kh. R.,Aliev, N. S.

, p. 340 - 344 (2007/10/02)

The alkylation of the potassium and triethylammonium salts of benzoxazolinones and benzoxazolinethiones with α-halo carbonyl compounds has been studied.The reaction takes place at the less electronegative atoms of the ambident benzoxazolinone and benzoxazolinethione anions.On the nitration of 3-phenacylbenzoxazoline moiety of the molecule.

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