Boc-Nva-OH

Modify Date: 2024-01-02 21:11:31

Boc-Nva-OH Structure
Boc-Nva-OH structure
Common Name Boc-Nva-OH
CAS Number 53308-95-5 Molecular Weight 217.262
Density 1.1±0.1 g/cm3 Boiling Point 348.3±25.0 °C at 760 mmHg
Molecular Formula C10H19NO4 Melting Point 43-47ºC
MSDS Chinese USA Flash Point 164.4±23.2 °C

 Use of Boc-Nva-OH


Boc-Nva-OH is a valine derivative[1].

 Names

Name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid
Synonym More Synonyms

 Boc-Nva-OH Biological Activity

Description Boc-Nva-OH is a valine 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 1.1±0.1 g/cm3
Boiling Point 348.3±25.0 °C at 760 mmHg
Melting Point 43-47ºC
Molecular Formula C10H19NO4
Molecular Weight 217.262
Flash Point 164.4±23.2 °C
Exact Mass 217.131409
PSA 75.63000
LogP 2.16
Vapour Pressure 0.0±1.6 mmHg at 25°C
Index of Refraction 1.462
Storage condition 0-6°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves
Hazard Codes Xi
Safety Phrases 24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924199090

 Synthetic Route

~67%

Boc-Nva-OH Structure

Boc-Nva-OH

CAS#:53308-95-5

Literature: Naskar, Jishu; Roy, Subhasish; Joardar, Anindita; Das, Sumantra; Banerjee, Arindam Organic and Biomolecular Chemistry, 2011 , vol. 9, # 19 p. 6610 - 6615

~98%

Boc-Nva-OH Structure

Boc-Nva-OH

CAS#:53308-95-5

Literature: Tetrahedron Asymmetry, , vol. 17, # 13 p. 1995 - 1999

~%

Boc-Nva-OH Structure

Boc-Nva-OH

CAS#:53308-95-5

Literature: Tetrahedron Letters, , vol. 28, # 48 p. 6069 - 6072

~%

Boc-Nva-OH Structure

Boc-Nva-OH

CAS#:53308-95-5

Literature: Tetrahedron Letters, , vol. 28, # 48 p. 6069 - 6072

~%

Boc-Nva-OH Structure

Boc-Nva-OH

CAS#:53308-95-5

Literature: Tetrahedron Letters, , vol. 28, # 48 p. 6069 - 6072

~%

Boc-Nva-OH Structure

Boc-Nva-OH

CAS#:53308-95-5

Literature: Tetrahedron Letters, , vol. 28, # 48 p. 6069 - 6072

~%

Boc-Nva-OH Structure

Boc-Nva-OH

CAS#:53308-95-5

Literature: Tetrahedron Letters, , vol. 28, # 48 p. 6069 - 6072

~%

Boc-Nva-OH Structure

Boc-Nva-OH

CAS#:53308-95-5

Literature: Tetrahedron Letters, , vol. 28, # 48 p. 6069 - 6072

~%

Boc-Nva-OH Structure

Boc-Nva-OH

CAS#:53308-95-5

Literature: Tetrahedron, , vol. 47, # 29 p. 5453 - 5462

 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

More Articles
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...

 Synonyms

BOC-L-NVA-OH
(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)pentanoic acid
N-(tert-Butoxycarbonyl)-L-norvaline
MFCD00037268
BOC-NVA-OH
L-Norvaline, N-[(1,1-dimethylethoxy)carbonyl]-
Boc-L-Norvaline
N-BOC-L-NORVALINE
RARECHEM EM WB 0170
BOC-NORVALINE
Boc-L-norvaline-OH
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-norvaline
BOC-1-NORVALINE
N-[(1,1-Dimethylethoxy)carbonyl]-L-methionine
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