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CAS

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138548-39-7

2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-1-[(1-oxopropoxy)methyl]-5-phenyl-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138548-39-7 Structure

  • Basic information

    1. Product Name: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-1-[(1-oxopropoxy)methyl]-5-phenyl-, (R)-
    2. Synonyms:
    3. CAS NO:138548-39-7
    4. Molecular Formula: C16H18N2O5
    5. Molecular Weight: 318.329
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138548-39-7.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: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-1-[(1-oxopropoxy)methyl]-5-phenyl-, (R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-1-[(1-oxopropoxy)methyl]-5-phenyl-, (R)-(138548-39-7)
    11. EPA Substance Registry System: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-1-[(1-oxopropoxy)methyl]-5-phenyl-, (R)-(138548-39-7)

  • 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: 138548-39-7(Hazardous Substances Data)

138548-39-7 Usage

Molecular Structure

2,4,6(1H,3H,5H)-Pyrimidinetrione core with a complex arrangement of atoms.

Pyrimidine Ring

A six-membered heterocyclic ring, which includes three oxygen atoms.

Substitution

The pyrimidine ring is substituted with an ethyl group and a (R)-5-ethyl-1-[(1-oxopropoxy)methyl]-5-phenyl group.

Stereochemistry

The compound has an (R) configuration, indicating the specific spatial arrangement of its atoms.

Potential Applications

Possible uses in pharmaceuticals or other industries due to its unique structure and properties.

Further Research

Additional studies and testing are required to fully understand its potential and possible applications.

Check Digit Verification of cas no

The CAS Registry Mumber 138548-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,4 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 138548-39:
(8*1)+(7*3)+(6*8)+(5*5)+(4*4)+(3*8)+(2*3)+(1*9)=157
157 % 10 = 7
So 138548-39-7 is a valid CAS Registry Number.

138548-39-7SDS

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 (R)-5-ethyl-5-phenyl-1-(propionyloxymethyl)barbital

1.2 Other means of identification

Product number -
Other names N-propionyloxymethylphenobarbital

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:138548-39-7 SDS

138548-39-7Relevant articles and documents

Lipase-catalyzed enantioselective synthesis of optically active mephrobarbital, hexobarbital and febarbamate

Murata,Uchida,Achiwa

, p. 2605 - 2609 (2007/10/02)

Chiral 5,5-disubstituted N-acyloxymethylbarbiturates have been obtained in 40-99% optical yields by lipase-catalyzed hydrolyses of 5,5-disubstituted N,N'-bisacyloxymethylbarbiturates in H2O-saturated diisopropyl ether. These chiral barbiturates

Lipase-catalyzed Enantioselective Hydrolysis of N-Acyloxymethyl Groups in Organic Solvent: Syntheses of Chiral 5,5-Disubstituted 1-Methylbarbiturates

Murata, Masakazu,Achiwa, Kazuo

, p. 6763 - 6766 (2007/10/02)

Chiral 5,5-disubstituted N-acyloxymethylbarbiturates have been obtained in 40-99percent optical yields by lipase-catalyzed hydrolyses of 5,5-disubstituted bisacyloxymethylbarbiturates in H2O-saturated diisopropyl ether.These chiral barbiturates were readi

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