Home > Compound List > Product Information
(R)-1,4-Dioxaspiro[4.5]decane-2-carboxaldehyde_Molecular_structure_CAS_78008-36-3)
Click picture or here to close

(R)-1,4-Dioxaspiro[4.5]decane-2-carboxaldehyde

Catalog No. 543039 Name Sigma Aldrich
CAS Number 78008-36-3 Website http://www.sigmaaldrich.com
M. F. C9H14O3 Telephone 1-800-521-8956
M. W. 170.20566 Fax
Purity Email
Storage Chembase ID: 151123

SYNONYMS

Title
(R)-1,4-二氧杂螺[4.5]癸烷-2-甲醛
IUPAC name
(2R)-1,4-dioxaspiro[4.5]decane-2-carbaldehyde
IUPAC Traditional name
(2R)-1,4-dioxaspiro[4.5]decane-2-carbaldehyde
Synonyms
(R)-2,3-Cyclohexylideneglyceraldehyde
O,O-Cyclohexylidene-(R)-glyceraldehyde
(R)-Cyclohexylideneglyceraldehyde
2,3-O-Cyclohexylidene-D-glyceraldehyde

DATABASE IDS

PubChem SID 24878656
MDL Number MFCD03093997
CAS Number 78008-36-3

PROPERTIES

Empirical Formula (Hill Notation) C9H14O3
Density 1.108 g/mL at 25 °C(lit.)
Optical Rotation [α]/D 60±10° in chloroform
Refractive Index n20/D 1.472(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Application
Used as a building block.6
Reactant for:
• Proline-catalyzed Diels Alder reaction1
• Stereodivergent synthesis of carbahexofuranoses employing a Wittig olefination-Claisen rearrangement protocol2
• Wittig reactions3
• Crotylation reactions4
• Asymmetric synthesis of Goniothalesdiol A via stereocontrolled allylation and base-catalyzed oxy-Michael addition5
Other Notes
Contains varying amounts of polymer
Packaging
1 g in glass bottle
Description (简体中文)
Application
作为结构单元。6
Reactant for:
• Proline-catalyzed Diels Alder reaction1
• Stereodivergent synthesis of carbahexofuranoses employing a Wittig olefination-Claisen rearrangement protocol2
• Wittig reactions3
• Crotylation reactions4
• Asymmetric synthesis of Goniothalesdiol A via stereocontrolled allylation and base-catalyzed oxy-Michael addition5
Other Notes
含不定量的聚合物
包装
1 g in glass bottle

REFERENCES