1-Pyrenecarboxaldehyde
Names
[ CAS No. ]:
3029-19-4
[ Name ]:
1-Pyrenecarboxaldehyde
[Synonym ]:
1-pyrenealdehyde
1-Pyrenecarboxaldehyde
Pyrenecarboxaldehyde
pyrenecarbaldehyde
pyrene-1-aldehyde
Pyrene-1-carbaldehyde
1-Pyrenecarbaldehyde
1-Pyrene-carboxaldehyde
pyrene-1-carboxaldehyde
1-Formylpyrene
MFCD00004139
3-Formylpyrene
EINECS 221-196-6
Chemical & Physical Properties
[ Density]:
1.3±0.1 g/cm3
[ Boiling Point ]:
438.2±14.0 °C at 760 mmHg
[ Melting Point ]:
123-126 °C(lit.)
[ Molecular Formula ]:
C17H10O
[ Molecular Weight ]:
230.261
[ Flash Point ]:
294.6±6.3 °C
[ Exact Mass ]:
230.073166
[ PSA ]:
17.07000
[ LogP ]:
4.59
[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C
[ Index of Refraction ]:
1.875
MSDS
Toxicological Information
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- UR2450200
- CHEMICAL NAME :
- 1-Pyrenecarboxaldehyde
- CAS REGISTRY NUMBER :
- 3029-19-4
- LAST UPDATED :
- 199410
- DATA ITEMS CITED :
- 1
- MOLECULAR FORMULA :
- C17-H10-O
- MOLECULAR WEIGHT :
- 230.27
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
MUTATION DATA
- TYPE OF TEST :
- Mutation in microorganisms
- TEST SYSTEM :
- Bacteria - Salmonella typhimurium
- DOSE/DURATION :
- 50 ug/plate
- REFERENCE :
- MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 157,149,1985
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi:Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ RTECS ]:
UR2450200
[ HS Code ]:
2912299000
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2912299000
[ Summary ]:
2912299000. other cyclic aldehydes without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%
Articles
Orig. Life Evol. Biosph. 42(4) , 295-306, (2012)
Aromatic molecules delivered to the young Earth during the heavy bombardment phase in the early history of our solar system were likely to be among the most abundant and stable organic compounds avail...
Fluorescent imino and secondary amino chitosans as potential sensing biomaterials.Carbohydr. Polym. 123 , 288-96, (2015)
A variety of fluorescent imino and secondary amino chitosans were synthesized under very mild conditions by reaction of the biopolymer amino functions with aromatic aldehydes in an acidified methanoli...
Ratiometric fluorescence sensing and intracellular imaging of Al3+ ions driven by an intramolecular excimer formation of a pyrimidine-pyrene scaffold.Dalton Trans. 42(14) , 4757-63, (2013)
An Al(3+) selective ratiometric fluorescent probe (L) has been synthesized by condensation of 4,5-diaminopyrimidine with 1-pyrenecarboxaldehyde. The structure of L has been confirmed by single crystal...