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2-(Hydroxy-phenyl-methyl)-1-phenyl-pent-4-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134853-08-0 Structure
  • Basic information

    1. Product Name: 2-(Hydroxy-phenyl-methyl)-1-phenyl-pent-4-en-1-one
    2. Synonyms: 2-(Hydroxy-phenyl-methyl)-1-phenyl-pent-4-en-1-one
    3. CAS NO:134853-08-0
    4. Molecular Formula:
    5. Molecular Weight: 266.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134853-08-0.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: 2-(Hydroxy-phenyl-methyl)-1-phenyl-pent-4-en-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(Hydroxy-phenyl-methyl)-1-phenyl-pent-4-en-1-one(134853-08-0)
    11. EPA Substance Registry System: 2-(Hydroxy-phenyl-methyl)-1-phenyl-pent-4-en-1-one(134853-08-0)
  • 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: 134853-08-0(Hazardous Substances Data)

134853-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134853-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,5 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 134853-08:
(8*1)+(7*3)+(6*4)+(5*8)+(4*5)+(3*3)+(2*0)+(1*8)=130
130 % 10 = 0
So 134853-08-0 is a valid CAS Registry Number.

134853-08-0Downstream Products

134853-08-0Relevant articles and documents

A novel sunscreen agent having antimelanoma activity

Nogueira, Marisa A.,Magalhaes, Eva G.,Magalhaes, Aderbal F.,Biloti, Debora N.,Laverde Jr., Antonio,Pessine, Francisco B.T.,Carvalho, Joao E.,Kohn, Luciana K.,Antonio, Marcia A.,Marsaioli, Anita J.

, p. 1163 - 1169 (2003)

A novel series of eight dibenzoylmethane derivatives having both sunscreen and cytotoxic activity has been obtained by derivatizing commercial dibenzoyl methanes. Four human cancer cell lines (MCF 7 (breast), NCI ADR (breast expressing the multidrug resis

Photochemically and Thermally Induced Free-Radical Reactions of α,β-Epoxy Ketones with Tributyltin Hydride: Selective Ca-O Bond Cleavage of Oxiranylmethyl Radicals Derived from α,β-Epoxy Ketones

Hasegawa, Eietsu,Ishiyama, Kenyuki,Kato, Tomoyasu,Horaguchi, Takaaki,Shimizu, Takahachi,et al.

, p. 5352 - 5359 (2007/10/02)

Free-radical reactions of α,β-epoxy ketones with tributyltin hydride have been studied.These substances were selectively converted to β-hydroxy ketones under both photochemical and thermal conditions.The photoreaction is initiated by hydrogen abstraction of an epoxy ketone triplet from tributyltin hydride, while azoisobutyronitrile is used as an initiator for the thermal reaction.In general, the photoreaction conditions are particularly useful for aroyl-substituted epoxy ketones while the thermal conditions are applicable to a variety of epoxy ketones.It was also found that the epoxy esters and epoxy alcohols did not undergo the ring-opening reaction under the similar conditions.Tributyltin radical attack on the carbonyl of epoxy ketones is a key process for both the photoreaction and the thermal reaction.Regioselective ring opening of the resulting oxiranylmethyl radical finally produces β-hydroxy ketones.In order to capture the free-radical intermediates, the reaction of epoxy ketones with allyltributyltin was conducted.The isolation of α-allylated β-hydroxy ketones is interpreted by the involvement of a novel 1,5-tributyltin transfer.

Free radical trapping of α-keto radicals derived from α,β-epoxy ketones via photoinduced single electron transfer process

Hasegawa, Eietsu,Ishiyama, Kenyuki,Horaguchi, Takaaki,Shimizu, Takahachi

, p. 2029 - 2032 (2007/10/02)

Irradiation of aromatic α,β-epoxy ketones in the presence of allyltributyltin afforded α-allyl-β-hydroxy ketones by a single electron transfer mechanism.

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