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CAS

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144152-29-4

Ethanone, 1-[2-(acetyloxy)-5-hydroxyphenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144152-29-4 Structure

  • Basic information

    1. Product Name: Ethanone, 1-[2-(acetyloxy)-5-hydroxyphenyl]-
    2. Synonyms:
    3. CAS NO:144152-29-4
    4. Molecular Formula: C10H10O4
    5. Molecular Weight: 194.187
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144152-29-4.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: Ethanone, 1-[2-(acetyloxy)-5-hydroxyphenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-[2-(acetyloxy)-5-hydroxyphenyl]-(144152-29-4)
    11. EPA Substance Registry System: Ethanone, 1-[2-(acetyloxy)-5-hydroxyphenyl]-(144152-29-4)

  • 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: 144152-29-4(Hazardous Substances Data)

144152-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144152-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,1,5 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 144152-29:
(8*1)+(7*4)+(6*4)+(5*1)+(4*5)+(3*2)+(2*2)+(1*9)=104
104 % 10 = 4
So 144152-29-4 is a valid CAS Registry Number.

144152-29-4SDS

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 2-acetoxy-5-hydroxyacetophenone

1.2 Other means of identification

Product number -
Other names -

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:144152-29-4 SDS

144152-29-4Relevant articles and documents

Base-Induced Chemiluminescence of Acetoxy-Substituted Benzofuran Dioxetanes by an Intramolecular Electron Transfer (CIEEL) Mechanism

Adam, Waldemar,Schulz, Manfred H.

, p. 2455 - 2462 (2007/10/02)

Tetraphenylporphine-sensitized photooxygenation of acetoxy-substituted benzofuran derivatives 2 afforded the corresponding benzofuran dioxetanes 3.The base-induced decomposition of these dioxetanes was studied and shown to involve an intramolecular CIEEL

Regioselective hydrolysis of polyacetoxy aromatic ketones with lipases in organic solvents

Parmar, V S,Khanduri, C H,Tyagi, O D,Prasad, A K,Gupta, Suman,et al.

, p. 925 - 929 (2007/10/02)

Lipases from porcine pancreas (PPL) and Candida cylindracea (CCL) have been used for deacetylation of polyacetoxy aromatic ketones in organic solvents.A systematic study has been made to establish regioselectivity, effect of the nature of solvents and role of steric bulk on hydrolysable groups.High regioselectivity and effect of nature of solvents on the rate of the reactions have been observed.

Regioselective deacylation of polyacetoxy aryl-methyl ketones by lipases in organic solvents

Parmar,Prasad,Sharma,Singh,Pati,Gupta

, p. 6495 - 6498 (2007/10/02)

Lipases from porcine pancreas and Candida cylindracea, suspended in organic solvents have been used to study regioselective deacylation of polyacetoxy acetophenones. It has been observed that the hydrolysis of acetate groups at positions other than ortho

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