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1025839-59-1

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1025839-59-1 Usage

Common use

Reagent in organic synthesis

Structure

Ester derivative of propionic acid with a phenyl group and a tert-butoxycarbonylamino functional group

Reactivity

4,6-dimethoxy-[1,3,5]triazin-2-yl ester moiety is highly reactive and can undergo various chemical reactions

Applications

Used in the preparation of peptides and biologically active molecules for facilitating amide bond formation and other important reactions

Check Digit Verification of cas no

The CAS Registry Mumber 1025839-59-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,8,3 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1025839-59:
(9*1)+(8*0)+(7*2)+(6*5)+(5*8)+(4*3)+(3*9)+(2*5)+(1*9)=151
151 % 10 = 1
So 1025839-59-1 is a valid CAS Registry Number.

1025839-59-1SDS

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 (S)-4,6-dimethoxy-1,3,5-triazin-2-yl 2-((tert-butoxycarbonyl)amino)-3-phenylpropanoate

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:1025839-59-1 SDS

1025839-59-1Relevant articles and documents

A fast and efficient one-pot microwave assisted synthesis of variously di-substituted 1,2,4-oxadiazoles

Porcheddu, Andrea,Cadoni, Roberta,De Luca, Lidia

supporting information; experimental part, p. 7539 - 7546 (2011/12/03)

A one-pot two-step microwave assisted synthesis of variously disubstituted 1,2,4-oxadiazoles from carboxylic acids and amidoximes is reported. This methodology is characterized by short reaction times, is versatile, robust and high-yielding and allows for

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