109183-71-3

109183-71-3 structure

Name: Boc-Chg-OH
Chemical Name: (2S)-2-cyclohexyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid
CAS Number: 109183-71-3
Molecular Formula: C₁₃H₂₃NO₄
Molecular Weight: 257.326
Catalog: Biochemical Amino acids and their derivatives Glycine derivatives
Create Date: 2018-04-11 08:00:00
Modify Date: 2024-01-02 18:22:47
(S)-2-((tert-Butoxycarbonyl)amino)-2-cyclohexylacetic acid is a Glycine (HY-Y0966) derivative[1].

Name	(2S)-2-cyclohexyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid
Synonyms	Cyclohexaneacetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (αS)- N-Boc-Chg-OH N-Boc-L-cyclohexylglycine boc-cyclohexyl-gly-oh N-(tert-butoxycarbamoyl)-(L)-cyclohexylglycine (2S)-Cyclohexyl({[(2-methyl-2-propanyl)oxy]carbonyl}amino)acetic acid N-Boc-L-2-cyclohexylglycine (S)-2-((tert-Butoxycarbonyl)amino)-2-cyclohexylacetic acid Boc-L-Cyclohexylglycine N-(tert-Butoxycarbonyl)-L-2-cyclohexylglycine Cyclohexaneacetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]- MFCD05662179 N-Boc-2-Cyclohexyl-L-glycine Boc-cHexGly-OH (S)-tert-butoxycarbonylamino-cyclohexyl-acetic acid [(tert-Butoxycarbonyl)amino](cyclohexyl)acetic acid Boc-cyclohexylglycine Boc-(S)-2-Cyclohexylglycine AmbotzBAA1396 BOC-L-alpha-cyclohexylglycine Boc-L-α-cyclohexylglycine (2S)-[(tert-butoxycarbonyl)amino](cyclohexyl)ethanoic acid (2S)-[(tert-Butoxycarbonyl)amino](cyclohexyl)acetic acid Cyclohexyl({[(2-methyl-2-propanyl)oxy]carbonyl}amino)acetic acid N-Boc-2-Cyclohexylglycine Boc-Chg-OH

Description	(S)-2-((tert-Butoxycarbonyl)amino)-2-cyclohexylacetic acid is a Glycine (HY-Y0966) derivative[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
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.

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes	Xn
RIDADR	NONH for all modes of transport
WGK Germany	3

24424-99-5

14328-51-9

~91%

109183-71-3

Literature: Journal of Medicinal Chemistry, , vol. 36, # 1 p. 166 - 172

24424-99-5

~85%

109183-71-3

Literature: US5338726 A1, ; US 5338726 A

1070-19-5

14328-51-9

~78%

109183-71-3

Literature: Chemical and Pharmaceutical Bulletin, , vol. 29, # 6 p. 1644 - 1654

2935-35-5

109183-71-3

Literature: Journal of Medicinal Chemistry, , vol. 36, # 1 p. 166 - 172

116611-45-1

109183-71-3

Literature: Tetrahedron Letters, , vol. 35, # 2 p. 237 - 240

107202-39-1

109183-71-3

Literature: Tetrahedron Letters, , vol. 35, # 2 p. 237 - 240

54512-75-3

109183-71-3

Literature: Tetrahedron Letters, , vol. 35, # 2 p. 237 - 240

155905-75-2

109183-71-3

Literature: Tetrahedron Letters, , vol. 35, # 2 p. 237 - 240