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52060-75-0

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52060-75-0 Usage

General Description

1-(1,2-Dioxopropyl)-L-proline, methyl ester is a chemical compound that belongs to the class of proline derivatives. It is a methyl ester of L-proline, which is an amino acid commonly found in nature. 1-(1,2-DIOXOPROPYL)-L-PROLINE, METHYL ESTER has a dioxopropyl group attached to the proline molecule, which gives it unique properties and potential applications. It is often used in the field of organic synthesis and pharmaceutical research, due to its reactivity and potential as a building block in the synthesis of more complex molecules. Additionally, it may have potential uses in the development of pharmaceutical drugs or as a research tool in biochemistry and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 52060-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,6 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52060-75:
(7*5)+(6*2)+(5*0)+(4*6)+(3*0)+(2*7)+(1*5)=90
90 % 10 = 0
So 52060-75-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO4/c1-6(11)8(12)10-5-3-4-7(10)9(13)14-2/h7H,3-5H2,1-2H3/t7-/m0/s1

52060-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-1-(2-oxopropanoyl)pyrrolidine-2-carboxylate

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:52060-75-0 SDS

52060-75-0Relevant articles and documents

Amino acids and peptides, IX. Pyruvoyl amino acids

Hausler,Schmidt

, p. 145 - 151 (1974)

-

Asymmetric Catalytic Hydrogenations of N-Pyruvoyl-(S)-proline Esters

Munegumi, Toratane,Fujita, Manabu,Maruyama, Tetsuya,Shiono, Shozo,Takasaki, Michiaki,Harada, Kaoru

, p. 249 - 254 (2007/10/02)

Asymmetric catalytic hydrogenations of the entitled compounds were carried out over palladium on charcoal in various solvents to afford N--(S)-proline esters with a d.e.(=diastereoisomeric excess) of up to 59percent.The stereochemistry of the catalytic hydrogenation was explained by the "chelation mechanism." And the effects of temperature and bulkiness of the ester groups on the asymmetric induction were also described.

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