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Merck
CN

15533

Boc-Abu-OH

≥97.0% (HPLC)

Synonym(s):

(S)-2-(Boc-amino)butyric acid, Boc-L-2-aminobutyric acid

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About This Item

Linear Formula:
C2H5CH[NHCO2C(CH3)3]CO2H
CAS Number:
34306-42-8
Molecular Weight:
203.24
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
57647478
MDL number:
MFCD00037267
Beilstein/REAXYS Number:
6801706

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InChI

1S/C9H17NO4/c1-5-6(7(11)12)10-8(13)14-9(2,3)4/h6H,5H2,1-4H3,(H,10,13)(H,11,12)/t6-/m0/s1

SMILES string

CC[C@H](NC(=O)OC(C)(C)C)C(O)=O

InChI key

PNFVIPIQXAIUAY-LURJTMIESA-N

assay

≥97.0% (HPLC)

optical activity

[α]20/D −18.5±2°, c = 1% in methanol

reaction suitability

reaction type: Boc solid-phase peptide synthesis

application(s)

peptide synthesis

Quality Level

100

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCBD0758V
BCBH3766V
BCBB8665V
BCBB8665
1367683

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Fahd Boutouja et al.
Biomolecules, 10(11) (2020-11-19)
The changing accessibility of nutrient resources induces the reprogramming of cellular metabolism in order to adapt the cell to the altered growth conditions. The nutrient-depending signaling depends on the kinases mTOR (mechanistic target of rapamycin), which is mainly activated by

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