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(E)-2-(3-oxoprop-1-en-1-yl)phenyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 199934-50-4 Structure
  • Basic information

    1. Product Name: (E)-2-(3-oxoprop-1-en-1-yl)phenyl benzoate
    2. Synonyms: (E)-2-(3-oxoprop-1-en-1-yl)phenyl benzoate
    3. CAS NO:199934-50-4
    4. Molecular Formula:
    5. Molecular Weight: 252.269
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 199934-50-4.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: (E)-2-(3-oxoprop-1-en-1-yl)phenyl benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-2-(3-oxoprop-1-en-1-yl)phenyl benzoate(199934-50-4)
    11. EPA Substance Registry System: (E)-2-(3-oxoprop-1-en-1-yl)phenyl benzoate(199934-50-4)
  • 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: 199934-50-4(Hazardous Substances Data)

199934-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199934-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,9,3 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 199934-50:
(8*1)+(7*9)+(6*9)+(5*9)+(4*3)+(3*4)+(2*5)+(1*0)=204
204 % 10 = 4
So 199934-50-4 is a valid CAS Registry Number.

199934-50-4Downstream Products

199934-50-4Relevant articles and documents

Inhibition of human tumor growth by 2'-hydroxy- and 2'- benzoyloxycinnamaldehydes

Lee, Chang Woo,Hong, Dong Ho,Han, Sang Bae,Park, Se Hyung,Kim, Hyae Kyeong,Kwon, Byoung-Mog,Kim, Hwan Mook

, p. 263 - 266 (1999)

2'-Hydroxycinnamaldehyde (HCA) was isolated from Cinnamomum cassia Blume (Lauraceae) and 2'-benzoyloxycinnamaldehyde (BCA) was prepared by the reaction of HCA and benzoyl chloride. HCA and BCA strongly inhibited in vitro growth of 29 kinds of human cancer

Modular synthesis of (E)-cinnamaldehydes directly from allylarenes via a metal-free DDQ-mediated oxidative process

Xu, Ting-Ting,Jiang, Tao-Shan,Han, Xiao-Lan,Xu, Yuan-Hong,Qiao, Jin-Ping

, p. 5350 - 5358 (2018/08/03)

An efficient synthesis of (E)-cinnamaldehydes by a metal-free DDQ-mediated oxidative transformation of allylarenes was developed. The protocol provides a practical method to prepare diverse (E)-cinnamaldehydes with broad functional group tolerance in good to excellent yields, including easy access to natural products randainal and geranyloxy sinapyl aldehyde from plant extracts. Finally, the mechanism of a single-electron transfer process was proposed.

Composition for preventing cancer comprising 2'-benzoyl-oxycinnamaldehyde

-

Page/Page column 4, (2008/06/13)

Disclosed is a composition for preventing cancer comprising a compound represented by Chemical Formula 1, 2′-benzoyloxycinnamaldehyde (BCA). BCA has the effects of delaying tumor incidence and increasing immune cells in a transgenic mouse overexpressing H-ras oncogene playing a critical role in tumor cell growth. Thus, BCA is useful as a cancer preventive drug.

COMPOSITION FOR PREVENTING CANCER COMPRISING 2'-BENZOYL-OXYCINNAMALDEHYDE

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Page/Page column 11, (2008/06/13)

Disclosed is a composition for preventing cancer comprising a compound represented by Chemical Formula 1, 2??-benzoyloxycinnamaldehyde (BCA). BCA has the effects of delaying tumor incidence and increasing immune cells in a transgenic mouse overexpressing H-ras oncogene playing a critical role in tumor cell growth. Thus, BCA is useful as a cancer preventive drug.

Cinnamaldehydes inhibit cyclin dependent kinase 4/cyclin D1

Jeong, Ha-Won,Kim, Mi-Ran,Son, Kwang-Hee,Young Han, Mi,Ha, Ji-Hong,Garnier, Matthieu,Meijer, Laurent,Kwon, Byoung-Mog

, p. 1819 - 1822 (2007/10/03)

A series of cinnamaldehydes was synthesized for the study of inhibitory activity against cyclin dependent kinases (CDKs). A couple of compounds selectively inhibited cyclin D1-CDK4 with an IC50 value of 7-18 μM. (C) 2000 Elsevier Science Ltd. All rights reserved.

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