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Undecylenic aldehyde

Name: Undecylenic aldehyde
Brand: ALDRICH

95%

Synonym(s):

10-Undecenal

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About This Item

Linear Formula:

H₂C=CH(CH₂)₈CHO

CAS Number:

112-45-8

Molecular Weight:

168.28

EC Number:

203-973-1

MDL number:

MFCD00007032

UNSPSC Code:

12352100

PubChem Substance ID:

24848045

NACRES:

NA.22

vapor density

>1 (vs air)

Assay

95%

form

liquid

refractive index

n20/D 1.4427 (lit.)

bp

98-100 °C/3 mmHg (lit.)

density

0.84 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

[H]C(=O)CCCCCCCCC=C

InChI

1S/C11H20O/c1-2-3-4-5-6-7-8-9-10-11-12/h2,11H,1,3-10H2

InChI key

OFHHDSQXFXLTKC-UHFFFAOYSA-N

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Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H315,H317,H412

Precautionary Statements

P261 - P264 - P272 - P273 - P280 - P302 + P352

Hazard Classifications

Aquatic Chronic 3 - Skin Irrit. 2 - Skin Sens. 1B

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Preparation and diastereomeric separation of an (S)- and (R)-1-(methoxycarbonyl)tridec-10-yl glucoside derivative, a precursor for a monosaccharide constituent of resin glycosides.

Shigeru Kobayashi et al.

Carbohydrate research, 337(11), 1047-1053 (2002-06-01)

The 6-O-mesyl derivative of phenyl 1-thio-beta-D-glucopyranoside was prepared from D-glucose as a synthetic equivalent of a 6-deoxy-hexosyl donor. Racemic methyl 11-hydroxytetradecanoate (methyl convolvulinolate) was synthesized by Grignard reaction of propylmagnesium bromide with 10-undecenal followed by hydroboration. Both intermediates were coupled

Synthesis of new mono and bis amides projected as potential histone deacetylase (HDAC) inhibitors.

Terracciano S, et al.

Tetrahedron, 66(13), 2520-2528 (2010)

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