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L-Proline, 1-[N-[(1,1-dimethylethoxy)carbonyl]-L-seryl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58810-15-4

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58810-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58810-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,1 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58810-15:
(7*5)+(6*8)+(5*8)+(4*1)+(3*0)+(2*1)+(1*5)=134
134 % 10 = 4
So 58810-15-4 is a valid CAS Registry Number.

58810-15-4SDS

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 (2S)-1-[(2S)-3-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoyl]pyrrolidine-2-carboxylic acid

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:58810-15-4 SDS

58810-15-4Downstream Products

58810-15-4Relevant academic research and scientific papers

STAT DEGRADERS AND USES THEREOF

-

, (2021/09/26)

The present invention provides compounds, compositions thereof, and methods of using the same.

Preparation and biological evaluation of key fragments and open analogs of scleritodermin A

Sellanes, Diver,Campot, Francisco,Nú?ez, Ivana,Lin, Gerardo,Espósito, Pablo,Dematteis, Sylvia,Salda?a, Jenny,Domílnguez, Laura,Manta, Eduardo,Serra, Gloria

experimental part, p. 5384 - 5395 (2010/08/19)

The synthesis of key fragments of scleritodermin A, their assembly, and their biological evaluation as cytotoxic and anthelmintic were performed.Highlights of the synthetic route include formation of the a-ketoamide linkage and use of stereocontrolled reactions.Open analogs of this natural product were obtained using a convergent strategy.

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