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247634

Sigma-Aldrich

cis-5-Norbornene-endo-2,3-dicarboxylic anhydride

99%

Synonym(s):

cis-endo-5-Norbornene-2,3-dicarboxylic anhydride, cis-endo-Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic anhydride

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About This Item

Empirical Formula (Hill Notation):
C9H8O3
CAS Number:
Molecular Weight:
164.16
Beilstein:
83657
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.23

Assay

99%

mp

165-167 °C (lit.)

SMILES string

[H][C@@]12C3CC(C=C3)[C@]1([H])C(=O)OC2=O

InChI

1S/C9H8O3/c10-8-6-4-1-2-5(3-4)7(6)9(11)12-8/h1-2,4-7H,3H2/t4-,5+,6-,7+

InChI key

KNDQHSIWLOJIGP-UMRXKNAASA-N

Pictograms

Health hazardCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Resp. Sens. 1 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Chao-Bin Yeh et al.
European journal of medicinal chemistry, 45(9), 3981-3985 (2010-08-10)
Previous research indicates that cantharidin, norcantharidin and their analogues exhibit anticancer activity due to their inhibition of cancer cell lines such as HL60, HT29 and L1210. The anticancer activities of cantharidin, norcantharidin and their analogues involve the suppression of serine/threonine
Malcolm Driffield et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 35(6), 1200-1213 (2018-02-24)
The polymeric coating used in metal packaging such as cans for foods and beverages may contain residual amounts of monomers used in the production of the coating, as well as unreacted linear and cyclic oligomers. Traditionally, although designed for use

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