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L-Aspartic acid 4-tert-butyl ester, 98%|193944|3057-74-7

L-Aspartic acid 4-tert-butyl ester, 98%

Cat. No JK193944_25_G
J&K Chemical

Product Information

Product Name
L-Aspartic acid 4-tert-butyl ester, 98%
Brand Name
J&K
Product Number
193944
CAS
3057-74-7
Molecular Formula
C8H15NO4
Molecular Weight
189.21
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
H-Asp(OtBu)-OH
PubChem CID
7010570
IUPAC Name
(2S)-2-amino-4-(2-methylpropan-2-yl)oxy-4-oxobutanoic acid
InChI Key
MXWMFBYWXMXRPD-YFKPBYRVSA-N
SMILES
CC(C)(C)OC(=O)CC@@H(C(=O)O)N

Properties

Melting Point
189
Optical Activity
8° to 10° (C=1, H2O)

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Incorporation of Azide and Alkyne Functionalities into Peptides
Publication Name: Science of Synthesis
Publication Date: 2021

Hydrogenolysis of O-Benzyl Esters
Publication Name: Science of Synthesis
Publication Date: 2017

Ten Years of Adventures with Pd/C Catalysts: From Reductive Processes to Coupling Reactions
Publication Name: Synlett
Publication Date: 2014-01-27
DOI: 10.1055/s-0033-1340668

Reliable and Safe, Gram-Scale Hydrogenation and Hydrogenolysis of O-Benzyl Ether Groups with In Situ Pd0/C Catalyst
Publication Name: Synthesis
Publication Date: 2011-08-10
DOI: 10.1055/s-0030-1260167

Asymmetric Synthesis of Conformationally Constrained trans-2,3-Piperidinedicarboxylic Acid Derivatives
Publication Name: Synlett
Publication Date: 2007-02
DOI: 10.1055/s-2007-968029

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