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3-Penten-2-one, 5,5,5-trifluoro-4-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 453-33-8 Structure
  • Basic information

    1. Product Name: 3-Penten-2-one, 5,5,5-trifluoro-4-hydroxy-
    2. Synonyms: 3-Penten-2-one, 5,5,5-trifluoro-4-hydroxy-
    3. CAS NO:453-33-8
    4. Molecular Formula: C5H5F3O2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 453-33-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-Penten-2-one, 5,5,5-trifluoro-4-hydroxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Penten-2-one, 5,5,5-trifluoro-4-hydroxy-(453-33-8)
    11. EPA Substance Registry System: 3-Penten-2-one, 5,5,5-trifluoro-4-hydroxy-(453-33-8)
  • 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: 453-33-8(Hazardous Substances Data)

453-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 453-33-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 453-33:
(5*4)+(4*5)+(3*3)+(2*3)+(1*3)=58
58 % 10 = 8
So 453-33-8 is a valid CAS Registry Number.

453-33-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1-trifluoro-2,4-pentanedione enol

1.2 Other means of identification

Product number -
Other names trifluoromethylacetylacetone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:453-33-8 SDS

453-33-8Downstream Products

453-33-8Relevant articles and documents

Highly enantioselective construction of 3-hydroxy oxindoles through a decarboxylative aldol addition of trifluoromethyl α-fluorinated gem-diols to n-benzyl isatins

Saidalimu, Ibrayim,Fang, Xiang,He, Xiao-Peng,Liang, Jing,Yang, Xueyan,Wu, Fanhong

, p. 5566 - 5570 (2013)

An organocatalytic asymmetric direct aldol addition reaction that involves cleavage of a carbon-carbon bond through the release of trifluoroacetate was developed. The protocol is wide in scope, generating the desired oxindoles of biological interest in nearly quantitative yields (up to 99 %) with excellent enantioselectivities (up to 98 % ee) and diastereoselectivities (up to 99:1 d.r.). Copyright

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