CAS 22838-58-0|Boc-D-Valine

Introduction:Basic information about CAS 22838-58-0|Boc-D-Valine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameBoc-D-Valine
CAS Number22838-58-0Molecular Weight217.262
Density1.1±0.1 g/cm3Boiling Point341.8±25.0 °C at 760 mmHg
Molecular FormulaC10H19NO4Melting Point164-165ºC
MSDSChineseUSAFlash Point160.5±23.2 °C

Names

Name(2R)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
SynonymMore Synonyms

Boc-D-Valine BiologicalActivity

Descriptiontert-Butoxycarbonyl-D-valine is a valine derivative[1].
Related CatalogResearch Areas >>OthersSignaling Pathways >>Others >>Others
In VitroAmino 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

Density1.1±0.1 g/cm3
Boiling Point341.8±25.0 °C at 760 mmHg
Melting Point164-165ºC
Molecular FormulaC10H19NO4
Molecular Weight217.262
Flash Point160.5±23.2 °C
Exact Mass217.131409
PSA75.63000
LogP1.98
Vapour Pressure0.0±1.6 mmHg at 25°C
Index of Refraction1.461
InChIKeySZXBQTSZISFIAO-SSDOTTSWSA-N
SMILESCC(C)C(NC(=O)OC(C)(C)C)C(=O)O
Storage condition2~8°C

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard CodesXi
Safety PhrasesS24/25
RIDADRNONH for all modes of transport
WGK Germany3
HS Code2924199090

Preparation


Customs

HS Code2924199090
Summary2924199090. 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

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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

(2S)-2-[(tert-butoxy)carbonylamino]-3-methylbutanoic acid
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-valine
(R)-2-((tert-Butoxycarbonyl)amino)-3-methylbutanoic acid
(S)-2-(Boc-amino)-3-methylbutyric acid
(2R)-2-[(TERT-BUTOXYCARBONYL)AMINO]-3-METHYLBUTANOIC ACID
Boc-D-Valine
N-t-Butoxycarbonyl-L-valine
BOC-L-Valine
tert-butyloxycarbonyl-D-valine
Boc-D-Val-OH
N-Boc-D-valine
L-Valine, N-[(1,1-dimethylethoxy)carbonyl]-
N-(tert-Butoxycarbonyl)-L-valin
Boc-L-Val-OH
MFCD00038282
Boc-L-Valine-OH
N-tert-Butoxycarbonyl-L-valine
N-t-butyloxycarbonyl-D-valine
N-α-(t-Butoxycarbonyl)-D-valine
(R)-Boc-Val-OH
(2S)-3-Methyl-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butanoic acid
N-Boc-valine
tBoc-DVal-OH
D-Valine, N-BOC protected
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-D-valine
N-(tert-Butoxycarbonyl)-D-valine
N-tert-Butyloxycarbonyl-L-valine
N-(tert-Butoxycarbonyl)-L-valine
D-Valine, N-[(1,1-dimethylethoxy)carbonyl]-
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