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5-methylproline is a non-proteinogenic amino acid, which means it is not commonly found in proteins. It is a derivative of proline, an essential amino acid, with an additional methyl group attached to the nitrogen atom. This modification can affect the chemical properties and reactivity of the molecule. 5-methylproline is not typically found in nature but can be synthesized in the laboratory. It has been studied for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique structural properties. The presence of the methyl group can influence the molecule's ability to form hydrogen bonds and its overall stability, which may be relevant in the design of new drugs or materials.

16639-15-9

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16639-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16639-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,3 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16639-15:
(7*1)+(6*6)+(5*6)+(4*3)+(3*9)+(2*1)+(1*5)=119
119 % 10 = 9
So 16639-15-9 is a valid CAS Registry Number.

16639-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-5-methylpyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-Carboxy-2-methyl-pyrrolidin

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:16639-15-9 SDS

16639-15-9Downstream Products

16639-15-9Relevant academic research and scientific papers

Scope and limitations in the use of N-(PhF)serine-derived cyclic sulfamidates for amino acid synthesis

Wei,Lubell

, p. 94 - 104 (2007/10/03)

Ring-opening of N-(PhF)serine-derived cyclic sulfamidate 17 was achieved with different nucleophiles (βketo esters, β-keto ketones, dimethyl malonate, nitroethane, sodium azide, imidazole, and potassium thiocyanate) to prepare a variety of amino acid anal

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