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Key Documents

15528

Sigma-Aldrich

Boc-Val-OH

≥99.0% (T)

Synonym(s):

(S)-2-(Boc-amino)-3-methylbutyric acid, N-(tert-Butoxycarbonyl)-L-valine, Boc-L-valine

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About This Item

Linear Formula:
(CH3)2CHCH(COOH)NHCOOC(CH3)3
CAS Number:
Molecular Weight:
217.26
Beilstein/REAXYS Number:
1711290
EC Number:
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥99.0% (T)

form

solid

optical activity

[α]20/D −6.2±0.5°, c = 1% in acetic acid

reaction suitability

reaction type: Boc solid-phase peptide synthesis
reaction type: C-H Activation
reagent type: ligand
reaction type: Peptide Synthesis

mp

77-80 °C (lit.)

application(s)

peptide synthesis

functional group

amine
carboxylic acid

SMILES string

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

InChI

1S/C10H19NO4/c1-6(2)7(8(12)13)11-9(14)15-10(3,4)5/h6-7H,1-5H3,(H,11,14)(H,12,13)/t7-/m0/s1

InChI key

SZXBQTSZISFIAO-ZETCQYMHSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Ye Sheng et al.
International journal of pharmaceutics, 487(1-2), 242-249 (2015-04-19)
Amino acid and dipeptide prodrugs have been developed to examine their potential in enhancing aqueous solubility and permeability as well as to bypass P-glycoprotein (P-gp) mediated cellular efflux of prednisolone. Prodrugs have been synthesized and identified with LC/MS/MS and NMR.

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