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Z-THR-NHNH2, also known as Z-threoninol, is a chemical compound utilized in the realm of organic chemistry, particularly for peptide synthesis. It serves as a protective agent for amino acids during the synthesis process, preventing undesired reactions from occurring in specific molecular regions. Characterized by its molecular formula C11H16N2O5, Z-THR-NHNH2 is typically found as a colorless to slightly yellow crystal or powder. Due to its potential health risks, it necessitates careful handling and storage.

49706-30-1

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49706-30-1 Usage

Uses

Used in Organic Chemistry:
Z-THR-NHNH2 is used as a protecting group for amino acids in peptide synthesis, ensuring that unwanted reactions are avoided in certain parts of the molecule.
Used in Pharmaceutical Industry:
Z-THR-NHNH2 is used as a key component in the development of peptide-based drugs, facilitating the synthesis of complex peptide structures with greater precision and control.
Used in Research and Development:
In academic and industrial research settings, Z-THR-NHNH2 is employed as a valuable tool for studying the properties and interactions of peptides, contributing to advancements in our understanding of peptide chemistry and its applications.

Check Digit Verification of cas no

The CAS Registry Mumber 49706-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,7,0 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 49706-30:
(7*4)+(6*9)+(5*7)+(4*0)+(3*6)+(2*3)+(1*0)=141
141 % 10 = 1
So 49706-30-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H11N3O2/c1-2(8)3(5)4(9)7-6/h2-3,8H,5-6H2,1H3,(H,7,9)/t2?,3-/m0/s1

49706-30-1SDS

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 Z-THR-NHNH2

1.2 Other means of identification

Product number -
Other names Z-THREONINE-NHNH2

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:49706-30-1 SDS

49706-30-1Relevant academic research and scientific papers

Process for preparing optically active oxazolidinone derivative

-

, (2008/06/13)

Disclosed is a process for preparing an optically active oxazolidinone derivative comprising allowing hydrazine to react on an optically active ester having a hydroxyl group at the 3-position which is represented by formula (II): wherein R1represents a lower alkyl group having 1 to 4 carbon atoms, a phenyl group, a methoxymethyl group, a benzyloxymethyl group, a benzyloxycarbonylaminomethyl group which may have a substituent or substituents on the benzene ring thereof, an acylaminomethyl group having 3 to 10 carbon atoms, or an alkyloxycarbonylaminomethyl group having 3 to 6 carbon atoms; R2and R3, which may be the same or different, each represent a hydrogen atom, a lower alkyl group having 1 to 4 carbon atoms, a phenyl group, an acetylaminomethyl group, a benzoylaminomethyl group, or a benzyl group; and * indicates an asymmetric carbon atom, and subjecting the resulting hydrazide to Curtius rearrangement.

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