CAS 13139-15-6|Boc-Leu-OH.H2O

Introduction：Basic information about CAS 13139-15-6|Boc-Leu-OH.H2O, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Boc-Leu-OH.H2O BiologicalActivity
3. Chemical & Physical Properties
4. Safety Information
5. Customs
6. Articles3
7. Synonyms

Common Name	Boc-Leu-OH.H2O
CAS Number	13139-15-6	Molecular Weight	231.289
Density	1.1±0.1 g/cm3	Boiling Point	339.7±44.0 °C at 760 mmHg
Molecular Formula	C₁₁H₂₁NO₄	Melting Point	85-87 °C
MSDS	ChineseUSA	Flash Point	159.2±28.4 °C

Names

Name	N(α)-t-butoxycarbonyl-L-leucine
Synonym	More Synonyms

Boc-Leu-OH.H2O BiologicalActivity

Description	Boc-L-Leu-OH is a leucine 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	1.1±0.1 g/cm3
Boiling Point	339.7±44.0 °C at 760 mmHg
Melting Point	85-87 °C
Molecular Formula	C₁₁H₂₁NO₄
Molecular Weight	231.289
Flash Point	159.2±28.4 °C
Exact Mass	231.147064
PSA	75.63000
LogP	2.99
Vapour Pressure	0.0±1.7 mmHg at 25°C
Index of Refraction	1.472
InChIKey	MDXGYYOJGPFFJL-QMMMGPOBSA-N
SMILES	CC(C)CC(NC(=O)OC(C)(C)C)C(=O)O
Storage condition	−20°C

Safety Information

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes	Xi,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%

Articles3

Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...

In situ fabrication of cleavable peptide arrays on polydimethylsiloxane and applications for kinase activity assays.

Anal. Chim. Acta 865 , 53-9, (2015)

Polydimethylsiloxane (PDMS) is widely used for microfabrication and bioanalysis; however, its surface functionalization is limited due to the lack of active functional groups and incompatibility with ...

Concise synthesis of PM-94128 and Y-05460M-A.

J. Org. Chem. 74(19) , 7566-9, (2009)

The enantioselective total synthesis of PM-94128, a potent cytotoxin of microbial origin, was accomplished by a concise nine-step sequence of reactions in 14% overall yield from N-Boc-l-leucine. The s...

Synonyms

N-Boc-L-leucine hydrate

(E)-N-{Hydroxy[(2-methyl-2-propanyl)oxy]methylene}-L-leucine

(S)-2-((tert-Butoxycarbonyl)amino)-4-methylpentanoic acid

MFCD00066067

L-LEUCINE-N-T-BOC:H2O

L-Leucine, N-[(1,1-dimethylethoxy)carbonyl]-

BOC-LEU

boc-leu-oh.h20

EINECS 236-073-2

N-tert-butoxycarbonyl-L-leucine

BOC-L-LEUCINE-OH

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

N-tert-butyloxycarbonyl-L-leucine

BOC-L-Leucine

N(alpha)-t-butoxycarbonyl-L-leucine

Boc-Leu-OH,H2O

Boc-Leu-OH.H2O

N-Boc-L-leucine Monohydrate

L-Leucine, N-[(1,1-dimethylethoxy)hydroxymethylene]-, (E)-

BOC-L-LEU-OH

BOC-LEU-OH

N-(tert-Butoxycarbonyl)-L-leucine Monohydrate

Boc-Leu-OH Monohydrate

N-Boc-L-leucine

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