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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

Quality Level

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

Certificates of Analysis (COA)

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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
Kendra Fein et al.
Carbohydrate polymers, 250, 117001-117001 (2020-10-15)
Cellulose nanofibrils (CNF) coatings are excellent grease barriers for biodegradable packaging. However, barrier properties are moisture sensitive, so hydrophobic components such as latexes or polymers are needed to impart moisture resistance, but incompatibility leads to poor dispersion. In this work
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
Claire Yu et al.
Biomaterials, 258, 120294-120294 (2020-08-18)
Recent advances in 3D bioprinting have transformed the tissue engineering landscape by enabling the controlled placement of cells, biomaterials, and bioactive agents for the biofabrication of living tissues and organs. However, the application of 3D bioprinting is limited by the

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