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331783

Sigma-Aldrich

trans-9,10-Dihydro-9,10-ethanoanthracene-11,12-dimethanol

96%

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Empirical Formula (Hill Notation):
C18H18O2
CAS Number:
Molecular Weight:
266.33
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

96%

form

solid

mp

203-205 °C (lit.)

SMILES string

OC[C@@H]1[C@@H](CO)C2c3ccccc3C1c4ccccc24

InChI

1S/C18H18O2/c19-9-15-16(10-20)18-12-6-2-1-5-11(12)17(15)13-7-3-4-8-14(13)18/h1-8,15-20H,9-10H2/t15-,16-,17?,18?/m1/s1

InChI key

JRUAWKGGVJZZQC-MRLCAUJQSA-N

Application

trans-9,10-Dihydro-9,10-ethanoanthracene-11,12-dimethanol was employed in the synthesis of dibenzo[b,f]oxepin scaffolds via Ullmann-type etheration reaction.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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An Efficient Synthesis of Dibenzo [b, f] oxepins by Ring-Closing Metathesis.
Bharath Y, et al
Asian Journal of Organic Chemistry, 2(10), 848-851 (2013)
Hui-Lung Sun et al.
Molecular cell, 80(4), 633-647 (2020-11-21)
N6-methyladenosine (m6A) is the most abundant mRNA modification and is installed by the METTL3-METTL14-WTAP methyltransferase complex. Although the importance of m6A methylation in mRNA metabolism has been well documented recently, regulation of the m6A machinery remains obscure. Through a genome-wide
İbrahim Avşar Ilik et al.
eLife, 9 (2020-10-24)
Nuclear speckles (NS) are among the most prominent biomolecular condensates. Despite their prevalence, research on the function of NS is virtually restricted to colocalization analyses, since an organizing core, without which NS cannot form, remains unidentified. The monoclonal antibody SC35

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