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CAS

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148114-19-6

4-[(4-tert-butylcyclohexyl)oxy]-4-oxobutanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 148114-19-6 Structure

  • Basic information

    1. Product Name: 4-[(4-tert-butylcyclohexyl)oxy]-4-oxobutanoic acid
    2. Synonyms: 4-[(4-tert-butylcyclohexyl)oxy]-4-oxobutanoic acid
    3. CAS NO:148114-19-6
    4. Molecular Formula: C14H24O4
    5. Molecular Weight: 256.33796
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148114-19-6.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: 4-[(4-tert-butylcyclohexyl)oxy]-4-oxobutanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[(4-tert-butylcyclohexyl)oxy]-4-oxobutanoic acid(148114-19-6)
    11. EPA Substance Registry System: 4-[(4-tert-butylcyclohexyl)oxy]-4-oxobutanoic acid(148114-19-6)

  • 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: 148114-19-6(Hazardous Substances Data)

148114-19-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148114-19-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,1,1 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 148114-19:
(8*1)+(7*4)+(6*8)+(5*1)+(4*1)+(3*4)+(2*1)+(1*9)=116
116 % 10 = 6
So 148114-19-6 is a valid CAS Registry Number.

148114-19-6Downstream Products

148114-19-6Relevant articles and documents

Convenient Synthesis of Alcohol O-Hemiesters using Isopropenyl Esters as Acylating Reagents: Synthesis of Hydrophilic Oxaunomycin 10-O-Hemiester Derivatives

Kita, Yasuyuki,Maeda, Hiroshi,Takahashi, Fumie,Fukui, Seiji

, p. 2639 - 2650 (2007/10/02)

Various types of alcohol O-hemiesters 7a-m were synthesized conveniently in good yield by reaction with isopropenyl esters 4a-f in the presence of a catalytic amount of conc.H2SO4 or toluene-p-sulfonic acid followed by selective deprotection of the terminal esters.This method was applied to a preparation of hydrophilic oxaunomycin 10-O-hemiester derivatives 14a,b and 19a-c.

A Convenient Synthesis of Dicarboxylic Monoesters using Isopropenyl Esters: Synthesis of Oxaunomycin Derivatives

Kita, Yasuyuki,Maeda, Hiroshi,Takahashi, Fumie,Fukui, Seiji

, p. 410 - 412 (2007/10/02)

Reaction of various types of alcohols with a novel type of acylating agent, the isopropenyl esters 2a-e in the presence of a catalytic amount of conc. sulfuric acid or toluene-p-sulfonic acid followed by selective deprotection of the terminal ester gives the monoesters 5a-i in good yields.

A NOVEL PREPARATION OF HEMISUCCINATES

Pouzar, Vladimir,Drasar, Pavel,Cerny, Ivan,Havel, Miroslav

, p. 501 - 507 (2007/10/02)

Hemisuccinates are prepared by condensation of succinic acid mono-2-(trimethylsilyl)ethyl ester with alcohols and subsequent aprotic removal of the protective group.

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