Boc-L-leucinol

Modify Date: 2024-01-02 21:21:20

Boc-L-leucinol Structure
Boc-L-leucinol structure
Common Name Boc-L-leucinol
CAS Number 82010-31-9 Molecular Weight 217.305
Density 1.0±0.1 g/cm3 Boiling Point 319.3±25.0 °C at 760 mmHg
Molecular Formula C11H23NO3 Melting Point N/A
MSDS Chinese USA Flash Point 146.9±23.2 °C

 Use of Boc-L-leucinol


Boc-Leucinol is a leucine derivative[1].

 Names

Name tert-butyl N-[(2S)-1-hydroxy-4-methylpentan-2-yl]carbamate
Synonym More Synonyms

 Boc-L-leucinol Biological Activity

Description Boc-Leucinol is a leucine derivative[1].
Related Catalog
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 1.0±0.1 g/cm3
Boiling Point 319.3±25.0 °C at 760 mmHg
Molecular Formula C11H23NO3
Molecular Weight 217.305
Flash Point 146.9±23.2 °C
Exact Mass 217.167801
PSA 58.56000
LogP 2.25
Vapour Pressure 0.0±1.5 mmHg at 25°C
Index of Refraction 1.454

 Safety Information

Personal Protective Equipment Eyeshields;Gloves
Hazard Codes T+
Safety Phrases S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924199090

 Synthetic Route

 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%

 Articles5

More Articles
Caputo, R. et al.

Tetrahedron 51 , 12337, (1995)

R. Caputo et al.

Tetrahedron Lett. 36 , 167, (1995)

Donner, B.G.

Tetrahedron Lett. 36 , 1223, (1995)

 Synonyms

(1S)-N-(t-butoxycarbonyl)-1-isobutyl-2-hydroxyethylamine
Carbamic acid, N-[(1S)-1-(hydroxymethyl)-3-methylbutyl]-, 1,1-dimethylethyl ester
(2S)-2-(t-butoxycarbonylamino)-4-methylpentanol
MFCD00076950
(S)-2-(tert-butoxycarbonylamino)-4-methyl-1-pentanol
2-Methyl-2-propanyl [(2S)-1-hydroxy-4-methyl-2-pentanyl]carbamate
Boc-Leu-ol
Boc-L-leucinol
tert-Butyl [(2S)-1-hydroxy-4-methylpentan-2-yl]carbamate
(S)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-methyl-1-pentanol
(2S)-2-(N-t-butoxycarbonylamino)-4-methylpentanol
tert-Butyl [(1S)-1-(hydroxymethyl)-3-methylbutyl]carbamate
N-Boc-L-leucinol
Boc-Leucinol
L-N-Boc-leucinol
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