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270596-47-9

270596-47-9 Structure

270596-47-9 Structure
IdentificationBack Directory
[Name]

BOC-(S)-3-AMINO-5-HEXYNOIC ACID
[CAS]

270596-47-9
[Synonyms]

Boc-b-HoPra-OH
Boc-β-HoPra-OH
BOC-BETA-HOPRA-OH
RARECHEM AK PT B003
Boc-β-HoGly(Propargyl)-OH
BOC-(PROPARGYL)GLY-(C*CH2)OH
Boc-beta-HoGly(Propargyl)-OH
Boc-(S)-3-amino-5-hexynoicaci
BOC-(S)-3-AMINO-5-HEXYNOIC ACID
BOC-L-BETA-HOMOPROPARGYLGLYCINE
(S)-3-(Boc-aMino)-5-hexynoic acid
(S)-3-(Boc-amino)-5-hexynoic acid
BOC-(S)-3-AMINO-5-HEXYNOIC ACID USP/EP/BP
N-T-BUTOXYCARBONYL-(S)-3-AMINO-5-HEXYNOIC ACID
(Tert-Butoxy)Carbonyl (S)-3-Amino-5-hexynoic acid
(S)-3-((tert-Butoxycarbonyl)amino)hex-5-ynoic acid
(3S)-3-{[(tert-butoxy)carbonyl]amino}hex-5-ynoic acid
(3S)-3-[[(tert-Butoxy)carbonyl]amino]-5-hexynoic acid
N-β-(t-Butoxycarbonyl)-β-propargyl-L-β-homophenylglycine
3-amino-2-[(2-methylpropan-2-yl)oxy-oxomethyl]-5-hexynoic acid
5-Hexynoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-, (3S)-
[Molecular Formula]

C11H17NO4
[MDL Number]

MFCD01861007
[MOL File]

270596-47-9.mol
[Molecular Weight]

227.26
Chemical PropertiesBack Directory
[Boiling point ]

386.7±37.0 °C(Predicted)
[density ]

1.129
[form ]

lumps
[pka]

4.31±0.10(Predicted)
[Optical Rotation]

[α]/D +26±2°, c = 1 in ethanol
[Major Application]

peptide synthesis
[InChI]

1S/C11H17NO4/c1-5-6-8(7-9(13)14)12-10(15)16-11(2,3)4/h1,8H,6-7H2,2-4H3,(H,12,15)(H,13,14)/t8-/m0/s1
[InChIKey]

QZRLAJLEZVWLOV-QMMMGPOBSA-N
[SMILES]

CC(C)(C)OC(=O)N[C@@H](CC#C)CC(O)=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[Storage Class]

6.1D - Non-combustible acute toxic Cat.3
toxic hazardous materials or hazardous materials causing chronic effects
[Hazard Classifications]

Acute Tox. 4 Oral
Hazard InformationBack Directory
[Uses]

peptide synthesis
[reaction suitability]

reaction type: click chemistry
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