284130
Psoralen
97%
Synonym(s):
6,7-Furanocoumarin, 7H-Furo[3,2-g]benzopyran-7-one, Ficusin, Furo[3,2-g]coumarin
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About This Item
Empirical Formula (Hill Notation):
C11H6O3
CAS Number:
Molecular Weight:
186.16
EC Number:
200-639-7
UNSPSC Code:
85151701
PubChem Substance ID:
Beilstein/REAXYS Number:
152784
MDL number:
InChI key
ZCCUUQDIBDJBTK-UHFFFAOYSA-N
InChI
1S/C11H6O3/c12-11-2-1-7-5-8-3-4-13-9(8)6-10(7)14-11/h1-6H
SMILES string
O=C1Oc2cc3occc3cc2C=C1
assay
97%
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Application
Photochemical reagent for the investigation of nucleic acid structure and function.
Disclaimer
Store in dark!
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Sens. 1
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Huricha Baigude et al.
Angewandte Chemie (International ed. in English), 51(24), 5880-5883 (2012-05-09)
Biochemical aspects of psoralen photochemotherapy.
A C Moor et al.
Clinics in dermatology, 14(4), 353-365 (1996-07-01)
Aurelio Reyes et al.
Nucleic acids research, 41(11), 5837-5850 (2013-04-19)
The observation that long tracts of RNA are associated with replicating molecules of mitochondrial DNA (mtDNA) suggests that the mitochondrial genome of mammals is copied by an unorthodox mechanism. Here we show that these RNA-containing species are present in living
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