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1569303-96-3

2-(3,4,5-trimethoxyphenylthio)benzoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1569303-96-3 Structure

  • Basic information

    1. Product Name: 2-(3,4,5-trimethoxyphenylthio)benzoxazole
    2. Synonyms:
    3. CAS NO:1569303-96-3
    4. Molecular Formula:
    5. Molecular Weight: 317.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1569303-96-3.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: 2-(3,4,5-trimethoxyphenylthio)benzoxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3,4,5-trimethoxyphenylthio)benzoxazole(1569303-96-3)
    11. EPA Substance Registry System: 2-(3,4,5-trimethoxyphenylthio)benzoxazole(1569303-96-3)

  • 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: 1569303-96-3(Hazardous Substances Data)

1569303-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1569303-96-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,3,0 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1569303-96:
(9*1)+(8*5)+(7*6)+(6*9)+(5*3)+(4*0)+(3*3)+(2*9)+(1*6)=193
193 % 10 = 3
So 1569303-96-3 is a valid CAS Registry Number.

1569303-96-3Downstream Products

1569303-96-3Relevant articles and documents

CuI promoted sulfenylation of organozinc reagents with arylsulfonyl chlorides

Fu, Ying,Su, Yuhu,Xu, Qin-Shan,Du, Zhengyin,Hu, Yulai,Wang, Ke-Hu,Huang, Danfeng

, p. 6018 - 6022 (2017/02/05)

A CuI promoted sulfenylation of organozinc reagents with arylsulfonyl chlorides/PPh3 has been explored. This reaction proceeded smoothly through an alkyl/aryl radical (generated from organometallics) under mild conditions and produced the desired sulfide products in excellent yields.

AROMATIC SULFIDE COMPOUNDS AND METHODS AND USE THEREOF

-

Paragraph 0168; 0189, (2015/11/03)

Described herein, inter alia, are aromatic sulfide compositions and methods for treating or preventing cancer using the same.

Diaryl and heteroaryl sulfides: Synthesis via sulfenyl chlorides and evaluation as selective anti-breast-cancer agents

Yonova, Ivelina M.,Osborne, Charlotte A.,Morrissette, Naomi S.,Jarvo, Elizabeth R.

, p. 1947 - 1953 (2014/04/03)

A mild protocol for the synthesis of diaryl and heteroaryl sulfides is described. In a one-pot procedure, thiols are converted to sulfenyl chlorides and reacted with arylzinc reagents. This method tolerates functional groups including aryl fluorides and chlorides, ketones, as well as N-heterocycles including pyrimidines, imidazoles, tetrazoles, and oxadiazoles. Two compounds synthesized by this method exhibited selective activity against the MCF-7 breast cancer cell line in the micromolar range.

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