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447854

Sigma-Aldrich

Diethyl 5-(hydroxymethyl)isophthalate

98%

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100 μL
$829.00

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100 μL
$829.00

About This Item

Linear Formula:
HOCH2C6H3-1,3-(CO2C2H5)2
CAS Number:
181425-91-2
Molecular Weight:
252.26
MDL number:
MFCD00239424
UNSPSC Code:
12352100
PubChem Substance ID:
24868368
NACRES:
NA.22

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Assay

98%

form

solid

mp

82-85 °C (lit.)

functional group

ester
hydroxyl

SMILES string

CCOC(=O)c1cc(CO)cc(c1)C(=O)OCC

InChI

1S/C13H16O5/c1-3-17-12(15)10-5-9(8-14)6-11(7-10)13(16)18-4-2/h5-7,14H,3-4,8H2,1-2H3

InChI key

AMRPMZYDTZVKTP-UHFFFAOYSA-N

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This Item
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Diethyl 5-(hydroxymethyl)isophthalate 98%

447854

Diethyl 5-(hydroxymethyl)isophthalate

4-(Hydroxymethyl)phenylacetic acid 98%

579610

4-(Hydroxymethyl)phenylacetic acid

3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chloride 98%

256234

3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chloride

(S)-(−)-5-Hydroxymethyl-2(5H)-furanone 98%

346861

(S)-(−)-5-Hydroxymethyl-2(5H)-furanone

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

-

form

solid

form

solid

form

solid

form

-

mp

82-85 °C (lit.)

mp

131-134 °C (lit.)

mp

142-144 °C (lit.)

mp

41-43 °C (lit.)

functional group

ester

functional group

carboxylic acid, hydroxyl

functional group

-

functional group

ester, hydroxyl

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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    SHBB5754V
    09129CH
    14720AE
    12928MD
    20526MO

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    Stefan Raddatz et al.
    Nucleic acids research, 30(21), 4793-4802 (2002-11-01)
    We report the synthesis of new phosphoramidite building blocks and their use for the modification of oligonucleotides with hydrazides. The reaction of these hydrazide oligonucleotides with active esters and aldehydes is demonstrated for solution conjugation and immobilization. Compared with the
    Surface adsorption of polar end-functionalised polystyrenes.
    Narrainen AP, et al.
    Soft Matter, 2(11), 981-985 (2006)
    Hydrophobic derivatives of 5-(hydroxymethyl) isophthalic acid that selectively induce apoptosis in leukemia cells but not in fibroblasts.
    Galkin A, et al.
    Drug Development Research, 69(4), 185-195 (2008)
    Gustav Boije af Gennäs et al.
    Journal of medicinal chemistry, 52(13), 3969-3981 (2009-05-15)
    Protein kinase C (PKC) is a widely studied molecular target for the treatment of cancer and other diseases. We have approached the issue of modifying PKC function by targeting the C1 domain in the regulatory region of the enzyme. Using

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