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(4R)-1-Methyl-4-propyl-L-proline Methyl Ester is a proline derivative, which is an essential amino acid that plays a crucial role in various biological processes. This specific compound is characterized by its unique structure, featuring a methyl group at the 1st position, a propyl group at the 4th position, and a methyl ester group attached to the carboxylic acid. It appears as a brown oil, indicating its油性 (oily) nature.

13380-39-7

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13380-39-7 Usage

Uses

Used in Pharmaceutical Industry:
(4R)-1-Methyl-4-propyl-L-proline Methyl Ester is used as an intermediate in the production of biosynthetic antibiotics. Its unique structure and properties make it a valuable component in the development of new antibiotics, which are essential for treating various bacterial infections.
Used in Chemical Synthesis:
As a proline derivative, (4R)-1-Methyl-4-propyl-L-proline Methyl Ester can also be utilized in chemical synthesis for the creation of other complex organic compounds. Its specific functional groups and structural features allow it to serve as a versatile building block in the synthesis of various molecules with potential applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 13380-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,8 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13380-39:
(7*1)+(6*3)+(5*3)+(4*8)+(3*0)+(2*3)+(1*9)=87
87 % 10 = 7
So 13380-39-7 is a valid CAS Registry Number.

13380-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R)-1-Methyl-4-propyl-L-proline Methyl Ester

1.2 Other means of identification

Product number -
Other names methyl (2S,4R)-1-methyl-4-propylpyrrolidine-2-carboxylate

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:13380-39-7 SDS

13380-39-7Relevant academic research and scientific papers

Synthesis of 1,2,3-triazole analogues of lincomycin

Collin, Marie-Pierre,Hobbie, Sven N.,Boettger, Erik C.,Vasella, Andrea

experimental part, p. 1838 - 1848 (2009/02/07)

In search for new antibiotics we replaced the amide moiety of lincomycin 1 by a 1,2,3-triazole ring. The 1,2,3-triazoles 10a-10k were obtained as single regioisomers by 'click reaction' of azide 5 with the alkyne 9k, derived from propyl hygric acid, and the alkyl, aryl, or cycloalkyl alkynes ribosomes 9a-9j. The new analogues proved inactive towards wild-type and A2058G mutant.

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