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25456-85-3

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25456-85-3 Usage

General Description

Z-Asn-OtBu, also known as N-tert-butoxycarbonyl-L-asparagine, is a chemical compound commonly used in the field of organic chemistry. It is a derivative of L-asparagine, an amino acid found in many proteins. Z-Asn-OtBu is frequently employed as a building block in peptide synthesis, where it serves as a protecting group to prevent unwanted reactions at specific functional groups within the molecule. Z-Asn-OtBu is also used in the production of pharmaceuticals and bioconjugates. Overall, Z-Asn-OtBu plays a critical role in the development of new molecules and materials with a wide range of applications in the fields of medicine, biotechnology, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 25456-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,5 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25456-85:
(7*2)+(6*5)+(5*4)+(4*5)+(3*6)+(2*8)+(1*5)=123
123 % 10 = 3
So 25456-85-3 is a valid CAS Registry Number.

25456-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (2S)-4-amino-4-oxo-2-(phenylmethoxycarbonylamino)butanoate

1.2 Other means of identification

Product number -
Other names Z-Asn-OtBu

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:25456-85-3 SDS

25456-85-3Relevant articles and documents

Synthesis of D- and L-5-oxaproline and of a new captopril analogue

Vasella,Voeffray

, p. 1241 - 1252 (2007/10/02)

-

Asymmetric Synthesis of a New Proline Analogue

Vasella, Andrea,Voeffray, Robert

, p. 97 - 98 (2007/10/02)

The 1,3-dipolar cycloaddition to ethylene of N-glycosylnitrones, formed in situ from the partially protected D-mannose- or D-ribose-oximes and various glyoxalates, gave compounds which could be transformed into both enantiomers of 3-t-butoxycarbonyl-isoxazolidine and derivatives thereof.

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