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138548-34-2

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138548-34-2 Usage

General Description

The chemical 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-methyl-1-[(1-oxopropoxy)methyl]-5-phenyl-, (R)- is a compound with the molecular formula C17H15NO5. It is a chiral molecule, with the (R)-enantiomer being the active form. 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-methyl-1-[(1-oxopropoxy)methyl]-5-phenyl-, (R)- is commonly used as a building block in pharmaceutical and agrochemical synthesis, as well as in the production of specialty chemicals. It has a variety of potential applications due to its unique structure, including use as an intermediate in the synthesis of pharmaceutical drugs and as a starting material for the preparation of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 138548-34-2 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 138548-34:
(8*1)+(7*3)+(6*8)+(5*5)+(4*4)+(3*8)+(2*3)+(1*4)=152
152 % 10 = 2
So 138548-34-2 is a valid CAS Registry Number.

138548-34-2SDS

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-methyl-5-phenyl-1-(propionyloxymethyl)barbital

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:138548-34-2 SDS

138548-34-2Relevant 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

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