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L-Proline, 2-(3-butenyl)(9CI) is a chemical compound that features the amino acid L-proline combined with a 3-butenyl group. It is recognized for its stability and versatility in chemical reactions, which makes it a valuable component in the development of new materials and drugs. This cyclic imino acid is also known for its potential biological activities, which are currently under investigation for applications in the pharmaceutical and biotechnology industries.

178752-81-3

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178752-81-3 Usage

Uses

Used in Organic Synthesis:
L-Proline, 2-(3-butenyl)(9CI) is used as a building block in organic synthesis for the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity contribute to the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, L-Proline, 2-(3-butenyl)(9CI) is utilized as a key component in the development of new drugs. Its potential biological activities are being researched for possible applications in medicine.
Used in Agrochemical Production:
L-Proline, 2-(3-butenyl)(9CI) also finds use in the agrochemical sector, where it serves as a building block for the synthesis of various agrochemicals, contributing to the development of new products for agricultural applications.
Used in Fine Chemicals Production:
L-Proline, 2-(3-butenyl)(9CI) is also used in the production of fine chemicals, where its unique properties allow for the creation of high-quality specialty chemicals for various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 178752-81-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,7,5 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 178752-81:
(8*1)+(7*7)+(6*8)+(5*7)+(4*5)+(3*2)+(2*8)+(1*1)=183
183 % 10 = 3
So 178752-81-3 is a valid CAS Registry Number.

178752-81-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-but-3-en-1-ylproline

1.2 Other means of identification

Product number -
Other names (S)-2-(3'-butenyl)proline

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:178752-81-3 SDS

178752-81-3Relevant academic research and scientific papers

Design, synthesis, and in vitro activity of peptidomimetic inhibitors of myeloid differentiation factor 88

Fantò, Nicola,Gallo, Grazia,Ciacci, Andrea,Semproni, Mauro,Vignola, Davide,Quaglia, Marco,Bombardi, Valentina,Mastroianni, Domenico,Zibella, M. Pia,Basile, Giancarlo,Sassano, Marica,Ruggiero, Vito,De Santis, Rita,Carminati, Paolo

, p. 1189 - 1202 (2008/09/20)

We describe the design and synthesis of a peptidomimetic library derived from the heptapeptide AC-RDVLPGT-NH2, belonging to the Toll/IL-1 receptor (TIR) domain of the adaptor protein MyD88 and effective in inhibiting its homodimerization. The a

Design, synthesis, and dopamine receptor modulating activity of spiro bicyclic peptidomimetics of L-prolyl-L-leucyl-glycinamide

Khalil, Ehab M.,Ojala, William H.,Pradhan, Ashish,Nair, Venugopalan D.,Gleason, William B.,Mishra, Ram K.,Johnson, Rodney L.

, p. 628 - 637 (2007/10/03)

In the present study, the synthesis of the 5.5.6. and 5.6.5. spiro bicyclic lactam PLG peptidomimetics, compounds 3 and 4, respectively, was undertaken. These peptidomimetics were designed to examine the following: (1) the effect that changing the size of

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