Skip to Content
Merck
CN

55262

4-[4-(1-Hydroxyethyl)-2-methoxy-5-nitrophenoxy]butyric acid

≥98.0% (HPLC), for peptide synthesis

Synonym(s):

Hydroxyethyl photolinker

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C13H17NO7
CAS Number:
175281-76-2
Molecular Weight:
299.28
NACRES:
NA.22
PubChem Substance ID:
57651521
UNSPSC Code:
12352106
MDL number:
MFCD01318869
Beilstein/REAXYS Number:
7717635

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

4-[4-(1-Hydroxyethyl)-2-methoxy-5-nitrophenoxy]butyric acid, ≥98.0% (HPLC)

InChI

1S/C13H17NO7/c1-8(15)9-6-11(20-2)12(7-10(9)14(18)19)21-5-3-4-13(16)17/h6-8,15H,3-5H2,1-2H3,(H,16,17)

SMILES string

COc1cc(C(C)O)c(cc1OCCCC(O)=O)[N+]([O-])=O

InChI key

DUIJUTBRRZCWRD-UHFFFAOYSA-N

assay

≥98.0% (HPLC)

form

powder

reaction suitability

reagent type: cross-linking reagent

mp

163-166 °C

Quality Level

100

Related Categories

Other Notes

Photolabile linker which can be bound to amino- and hydroxymethyl resins. Synthesis of sensitive acids

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000388818
0000388818
0000227736
0000227736
0000181605

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

D.L. Whitehouse et a
Tetrahedron Letters, 38, 7851-7851 (1997)
Christopher P. Holmes
The Journal of organic chemistry, 62(8), 2370-2380 (1997-04-18)
Both a model phenacyl and o-nitrobenzyl photolabile linker from the literature along with four new o-nitrobenzyl linkers were prepared and the kinetics of their photolytic cleavage examined in solution. The linkers were prepared by amidation of the carboxylic acid anchoring
Mime Kobayashi et al.
Journal of biomaterials science. Polymer edition, 30(13), 1161-1171 (2019-06-16)
We have developed biocompatible scaffolds that enable cell fate control with visible light. The scaffolds are based on synthetic collagen-like polypeptide, poly(prolyl-hydroxyprolyl-glycyl) {poly(Pro-Hyp-Gly)} which has been used for cosmetics and other healthcare applications. Bioactive peptides were conjugated to the scaffolds

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service