Fmoc-Thr(tBu)-OH

ALDRICH/47622 - ≥98.0% (HPLC)

Synonym: Fmoc-O-tert-butyl-L-threonine

CAS Number: 71989-35-0
Empirical Formula (Hill Notation): C₂₃H₂₇NO₅
Molecular Weight: 397.46
EC Number: 276-261-1
MDL Number: MFCD00077075
Linear Formula: C₂₃H₂₇NO₅
Product Type: Chemical

Catalog Number	PKG Qty.	Price	Quantity


45-47622-10G-F	10 g	$96.20 1/EA		Add To Favorites
45-47622-100G-F	100 g	$246.00 1/EA		Add To Favorites

Properties
Descriptions
Safety Info.
Basic Data

application(s)	peptide synthesis
assay	≥98.0% (HPLC)
functional group	amine
	carboxylic acid
	Fmoc
InChI	1S/C23H27NO5/c1-14(29-23(2,3)4)20(21(25)26)24-22(27)28-13-19-17-11-7-5-9-15(17)16-10-6-8-12-18(16)19/h5-12,14,19-20H,13H2,1-4H3,(H,24,27)(H,25,26)/t14-,20+/m1/s1
InChI key	LZOLWEQBVPVDPR-VLIAUNLRSA-N
optical activity	[α]20/D +16±1°, c = 1% in ethyl acetate
reaction suitability	reaction type: C-H Activation
	reaction type: Fmoc solid-phase peptide synthesis
	reagent type: ligand reaction type: Peptide Synthesis
SMILES string	C[C@@H](OC(C)(C)C)[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
storage temp.	2-8°C

Application:	Fmoc-Thr(tBu)-OH can be used to synthesize chlorofusin analogues via solid phase peptide synthesis. Additionally, it can serve as a protecting group for both the amine and the hydroxyl functions in solid-phase synthesis of complex depsipeptides.
General description:	Fmoc-Thr(tBu)-OH also known as Fmoc-O-tert-butyl-L-threonine, is commonly used as amino acid building block in peptide synthesis.
Packaging:	1, 10 g in glass bottle

Hazard Codes	N
Risk Statements	50/53
Safety Statements	60-61
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

Purity	≥98.0% (HPLC)
Storage Temp.	2-8°C
UNSPSC	12352209

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