Substance

ID:332043

Names and Identifiers
IUPAC name
piperidine-1-carbaldehyde
IUPAC Traditional name
N-formylpiperidine
Synonyms
N-Carbaldehyde piperidine1-甲酰哌啶哌啶-1-甲醛1-FormylpiperidineNFPPiperidine-1-carboxaldehyde
Registration numbers
CAS Number
MDL Number
Beilstein Number
EC Number
PubChem SID
Properties
Physical Property
Flash Point
215.6 °F
102 °C
Density
1.019 g/mL at 25 °C(lit.)
Refractive Index
n20/D 1.484(lit.)
Boiling Point
222 °C(lit.)
Vapor Pressure
0.1 mmHg ( 25 °C)
Safety Information
European Hazard Symbols
Harmful Harmful (Xn)
UN Number
2810
RTECS
TN0380000
Personal Protective Equipment
Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
RID/ADR
UN 2810 6.1/PG 3
German water hazard class
3
GHS Pictograms
GHS06
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
GHS Hazard statements
H302-H311-H315-H319-H335
MSDS Link
GHS Signal Word
Danger
Packing Group
3
Risk Statements
21/22-36/37/38
Safety Statements
26-36/37
Hazard Class
6.1
GHS Precautionary statements
P261-P280-P305+P351+P338-P312
Product Information
Empirical Formula (Hill Notation)
C6H11NO
Purity
99%
Molecule Details
Packaging
100, 500 g in glass bottle
Application
Reactant for:
• Direct amidation of azoles with formamides via metal-free C-H activation in the presence of tert-butyl perbenzoate1
• Vilsmeier-type reactions of pyrazoles with amides in the presence of phosphorous oxychloride2
• CO-free aminocarbonylation of N-substituted formamides with aryl iodides/bromides catalyzed by palladium acetate and Xantphos for synthesis of arylamides3
• Synthesis of alternating copolymers for organic photovoltaic applications4
• One-pot double functionalization of π-deficient heterocyclic lithium reagents5
• Synthesis of thermally stable piezofluorochromic aggregation-induced emission compounds6
Molecular Spectra
No Data Available
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References
No Data Available
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