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359653

Boc-Ile-OH

≥97%

Synonym(s):

N-(tert-Butoxycarbonyl)-L-isoleucine, Boc-L-isoleucine

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Size/SKUAvailabilityPrice
25 g

Available to ship TODAY

$143.00

About This Item

Linear Formula:
CH3CH2CH(CH3)CH(COOH)NHCOOC(CH3)3
CAS Number:
Molecular Weight:
231.29
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
236-074-8
MDL number:
Beilstein/REAXYS Number:
1711700

$143.00


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Quality Segment

assay

≥97%

optical activity

[α]20/D +2.7°, c = 2 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

66-69 °C (lit.)

application(s)

peptide synthesis

functional group

amine, carboxylic acid

SMILES string

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

InChI

1S/C11H21NO4/c1-6-7(2)8(9(13)14)12-10(15)16-11(3,4)5/h7-8H,6H2,1-5H3,(H,12,15)(H,13,14)/t7-,8-/m0/s1

InChI key

QJCNLJWUIOIMMF-YUMQZZPRSA-N


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This Item
47628
description

≥97%

description

≥98.0% (T)

functional group

carboxylic acid, amine

functional group

Fmoc, amine, carboxylic acid

assay

≥97%

assay

≥98.0% (T)

mp

66-69 °C (lit.)

mp

145-147 °C (lit.)

optical activity

[α]20/D +2.7°, c = 2 in acetic acid

optical activity

[α]20/D −12±1°, c = 1% in DMF

Quality Level

200

Quality Level

100

reaction suitability

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

reaction suitability

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


Storage Class

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

PPE (personal protective equipment)

Eyeshields, Gloves, type N95 (US)



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