N-Benzyl-N-(tert-butoxycarbonyl)glycine

Modify Date: 2024-01-17 17:41:17

N-Benzyl-N-(tert-butoxycarbonyl)glycine Structure
N-Benzyl-N-(tert-butoxycarbonyl)glycine structure
Common Name N-Benzyl-N-(tert-butoxycarbonyl)glycine
CAS Number 76315-01-0 Molecular Weight 265.305
Density 1.2±0.1 g/cm3 Boiling Point 409.5±34.0 °C at 760 mmHg
Molecular Formula C14H19NO4 Melting Point N/A
MSDS USA Flash Point 201.5±25.7 °C

 Use of N-Benzyl-N-(tert-butoxycarbonyl)glycine


2-(Benzyl(tert-butoxycarbonyl)amino)acetic acid is a Glycine (HY-Y0966) derivative[1].

 Names

Name 2-[benzyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]acetic acid
Synonym More Synonyms

 N-Benzyl-N-(tert-butoxycarbonyl)glycine Biological Activity

Description 2-(Benzyl(tert-butoxycarbonyl)amino)acetic acid is a Glycine (HY-Y0966) 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 1.2±0.1 g/cm3
Boiling Point 409.5±34.0 °C at 760 mmHg
Molecular Formula C14H19NO4
Molecular Weight 265.305
Flash Point 201.5±25.7 °C
Exact Mass 265.131409
PSA 66.84000
LogP 3.27
Vapour Pressure 0.0±1.0 mmHg at 25°C
Index of Refraction 1.535

 Safety Information

HS Code 2924299090

 Customs

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Synonyms

2-(Benzyl(tert-butoxycarbonyl)amino)acetic acid
N-Benzyl-N-(tert-butoxycarbonyl)glycine
N-benzyl-N-tert-butyloxycarbonylglycine
Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-(phenylmethyl)-
(N-benzyl-N-tert-butoxycarbonyl)aminoacetic acid
N-(tert-butoxycarbonyl)-N-benzylglycine
N-Bn-N-Boc-glycine
N-Benzyl-N-{[(2-methyl-2-propanyl)oxy]carbonyl}glycine
(benzyl-tert-butoxycarbonylamino)acetic acid
N-Boc-N-benzylglycine
Boc-(N-Bzl)Gly-OH