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Merck
모든 사진(1)

문서

47628

Sigma-Aldrich

Fmoc-Ile-OH

≥98.0% (T)

동의어(들):

N-(9-Fluorenylmethoxycarbonyl)-L-isoleucine, Fmoc-L-isoleucine

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About This Item

실험식(Hill 표기법):
C21H23NO4
CAS Number:
Molecular Weight:
353.41
Beilstein:
4716717
EC Number:
MDL number:
UNSPSC 코드:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26

분석

≥98.0% (T)

형태

solid

광학 활성

[α]20/D −12±1°, c = 1% in DMF

반응 적합성

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

mp

145-147 °C (lit.)

응용 분야

peptide synthesis

작용기

Fmoc
amine
carboxylic acid

저장 온도

2-8°C

SMILES string

CC[C@H](C)[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C21H23NO4/c1-3-13(2)19(20(23)24)22-21(25)26-12-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,13,18-19H,3,12H2,1-2H3,(H,22,25)(H,23,24)/t13-,19-/m0/s1

InChI key

QXVFEIPAZSXRGM-DJJJIMSYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


시험 성적서(COA)

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문서

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

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