CAS 13726-67-5|Boc-Asp-OH

Introduction：Basic information about CAS 13726-67-5|Boc-Asp-OH, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Boc-Asp-OH BiologicalActivity
3. Chemical & Physical Properties
4. Safety Information
5. Customs
6. Articles1
7. Synonyms

Common Name	Boc-Asp-OH
CAS Number	13726-67-5	Molecular Weight	353.327
Density	1.3±0.1 g/cm3	Boiling Point	609.3±55.0 °C at 760 mmHg
Molecular Formula	C₁₅H₁₉N₃O₇	Melting Point	116-118 °C(lit.)
MSDS	ChineseUSA	Flash Point	322.3±31.5 °C

Names

Name	Boc-Asp-OH
Synonym	More Synonyms

Boc-Asp-OH BiologicalActivity

Description	Boc-Asp-OH is an aspartic acid derivative[1].
Related Catalog	Research Areas >>OthersSignaling Pathways >>Others >>Others
In Vitro	Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References	[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Chemical & Physical Properties

Density	1.3±0.1 g/cm3
Boiling Point	609.3±55.0 °C at 760 mmHg
Melting Point	116-118 °C(lit.)
Molecular Formula	C₁₅H₁₉N₃O₇
Molecular Weight	353.327
Flash Point	322.3±31.5 °C
Exact Mass	353.122314
PSA	112.93000
LogP	2.05
Vapour Pressure	0.0±1.7 mmHg at 25°C
Index of Refraction	1.550
InChIKey	KAJBMCZQVSQJDE-YFKPBYRVSA-N
SMILES	CC(C)(C)OC(=O)NC(CC(=O)O)C(=O)O

Safety Information

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes	Xn
Risk Phrases	R20/21/22
Safety Phrases	26-36
RIDADR	NONH for all modes of transport
WGK Germany	3
HS Code	2924199090

Customs

HS Code	2924199090
Summary	2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles1

Aspartic acid-based modified PLGA–PEG nanoparticles for bone targeting: In vitro and in vivo evaluation

Acta Biomater. 10(11) , 4583-96, (2014)

Bone targeting NPs comprised of dendritic trimer of aspartic acid functionalized PLGA-PEG copolymers could be the foundation for hydrophobic-drug therapies.

Synonyms

(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)succinic acid

EINECS 237-294-7

tert-butyloxycarbonyl-L-aspartic acid

BOC-ASP

L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-

Boc-L-aspartic acid

L-Asparagine, N-[(1,1-dimethylethoxy)carbonyl]-, 4-nitrophenyl ester

N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-aspartic acid

BOC-L-ASP

N-t-butyloxycarbonyl-L-aspartic acid

BOC-ASPARTIC ACID

N-BOC-L-aspartic acid

L-Asparagine, N2-((1,1-dimethylethoxy)carbonyl)-, 4-nitrophenyl ester

N-Boc-aspartic acid

N-tert-Butoxycarbonyl-L-aspartic acid

tert-Butoxycarbonyl-L-aspartic acid

N-(tert-Butoxycarbonyl)-L-aspartic Acid

t-butoxycarbonyl-L-aspartic acid

Boc-L-Aspatic Acid

N-Boc-L-Asp-benzyl ester

MFCD00037279

N2-((1,1-Dimethylethoxy)carbonyl)-L-asparagine, 4-nitrophenyl ester

N-BOC-1-ASPARTICACID

4-Nitrophenyl N-(tert-butoxycarbonyl)-L-asparaginate

N-tert-Butyloxycarbonyl-L-aspartic acid

BOC-L-ASP-OH

Boc-D-Asp-OH

4-Nitrophenyl N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-asparaginate

BOC-L-Aspatic

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