CAS 4530-20-5|Boc-Gly-OH

Introduction:Basic information about CAS 4530-20-5|Boc-Gly-OH, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameBoc-Gly-OH
CAS Number4530-20-5Molecular Weight175.182
Density1.2±0.1 g/cm3Boiling Point315.9±25.0 °C at 760 mmHg
Molecular FormulaC7H13NO4Melting Point86-89 °C(lit.)
MSDSUSAFlash Point144.9±23.2 °C

Names

Namet-Butoxycarbonylglycine
SynonymMore Synonyms

Boc-Gly-OH BiologicalActivity

DescriptionBoc-Glycine is a Glycine (HY-Y0966) 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

Density1.2±0.1 g/cm3
Boiling Point315.9±25.0 °C at 760 mmHg
Melting Point86-89 °C(lit.)
Molecular FormulaC7H13NO4
Molecular Weight175.182
Flash Point144.9±23.2 °C
Exact Mass175.084457
PSA75.63000
LogP0.75
Vapour Pressure0.0±1.4 mmHg at 25°C
Index of Refraction1.460
InChIKeyVRPJIFMKZZEXLR-UHFFFAOYSA-N
SMILESCC(C)(C)OC(=O)NCC(=O)O
Storage condition-20°C
Water Solubilitysoluble

Safety Information

Personal Protective Equipmentdust mask type N95 (US);Eyeshields;Faceshields;Gloves
Hazard CodesXi:Irritant
Risk PhrasesR41
Safety PhrasesS26-S36/37/39-S39
RIDADRUN 2811 6.1/PG 3
WGK Germany3
Hazard Class6.1
HS Code2924199090

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%

Articles9

More Articles
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 ...

Accumulation of cell-penetrating peptides in large unilamellar vesicles: A straightforward screening assay for investigating the internalization mechanism.

Biopolymers 104 , 533-43, (2015)

The internalization of cell-penetrating peptides (CPPs) into liposomes (large unilamellar vesicles, LUVs) was studied with a rapid and robust procedure based on the quenching of a small fluorescent pr...

Optimization of the Ugi reaction using parallel synthesis and automated liquid handling.

J. Vis. Exp. (21) , doi:10.3791/942, (2008)

The optimization of a Ugi reaction involving the mixing of furfurylamine, benzaldehyde, boc-glycine and t-butylisocyanide is described. Triplicate runs of 48 parallel experiments are reported, varying...

Synonyms

N-(tert-Butoxycarbonyl)glycin
Glycine, N-[(1,1-dimethylethoxy)carbonyl]-
Boc-glycine
N-Boc-protected glycine
n-boc-glycine
boc-gly
N-(tert-butoxycarbonyl)glycine
Boc-Gly-OH
MFCD00002690
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}glycine
N-Boc-L-glycine
2-((tert-Butoxycarbonyl)amino)acetic acid
({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)acetic acid
Glycine, N-carboxy-, N-tert-butyl ester
N-Boc glycine
EINECS 224-864-5
CAS 13035-19-3|4-Piperidinamine
CAS 71989-20-3|Fmoc-Gln-OH
Recommended......
TOP