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Merck
CN

55730

Sigma-Aldrich

4-(羟基甲基)苯氧基乙酸

≥97.0%

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经验公式(希尔记法):
C9H10O4
CAS号:
分子量:
182.17
Beilstein:
5260336
MDL编号:
UNSPSC代码:
12352106
PubChem化学物质编号:
NACRES:
NA.22

检测方案

≥97.0%

反应适用性

reagent type: cross-linking reagent

mp

112-114 °C

官能团

carboxylic acid
hydroxyl

储存温度

−20°C

SMILES字符串

OCC1=CC=C(OCC(O)=O)C=C1

InChI

1S/C9H10O4/c10-5-7-1-3-8(4-2-7)13-6-9(11)12/h1-4,10H,5-6H2,(H,11,12)

InChI key

VUCNQOPCYRJCGQ-UHFFFAOYSA-N

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其他说明

用于根据"FMOC-聚酰胺"技术进行固相肽合成的键合剂

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

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E. Atherton et al.
Journal of the Chemical Society. Chemical Communications, 537-537 (1978)
A. Dryland et al.
Journal of the Chemical Society. Perkin Transactions 1, 125-125 (1986)
C T Bui et al.
Journal of peptide science : an official publication of the European Peptide Society, 6(10), 534-538 (2000-11-09)
A replacement of the acetic acid moiety by valeric acid within the 4-hydroxymethylphenoxyacetic acid (HMP) linker (Sheppard RC, Williams BJ. Acid-labile resin linkage agents for use in solid phase peptide synthesis. Int. J. Peptide Protein Res. 1982; 20: 451-454) significantly
Journal of the Chemical Society. Chemical Communications, 539-539 (1978)
R C Sheppard et al.
International journal of peptide and protein research, 20(5), 451-454 (1982-11-01)
Details are given of the preparation of two acid-labile peptide-resin linkage agents for use in solid phase peptide synthesis, viz. 4-hydroxymethylphenoxy-acetic acid and 3-methoxy-4-hydroxymethylphenoxyacetic acid. The latter is suitable for the preparation of peptide fragments bearing t-butyl-based side chain protecting

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