446440
5-Norbornene-2-carboxylic acid, mixture of endo and exo, predominantly endo
98%
Synonym(s):
2-Norbornene-5-carboxylic acid, Bicyclo[2.2.1]hept-2-ene-5-carboxylic acid
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About This Item
Empirical Formula (Hill Notation):
C8H10O2
CAS Number:
Molecular Weight:
138.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
refractive index
n20/D 1.494 (lit.)
bp
136-138 °C/14 mmHg (lit.)
density
1.129 g/mL at 25 °C (lit.)
functional group
carboxylic acid
SMILES string
OC(=O)C1C[C@H]2C[C@@H]1C=C2
InChI
1S/C8H10O2/c9-8(10)7-4-5-1-2-6(7)3-5/h1-2,5-7H,3-4H2,(H,9,10)/t5-,6+,7?/m1/s1
InChI key
FYGUSUBEMUKACF-JEAXJGTLSA-N
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Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Step-growth, radically mediated thiol-norbornene photopolymerization is used to create versatile, stimuli-responsive poly(ethylene glycol)-co-peptide hydrogels The reaction is cytocompatible and allows for the encapsulation of human mesenchymal stem cells with a viability greater than 95%. Cellular spreading is dictated via three-dimensional
A Convenient Practical Method for the Preparation of (-)-(1 S, 2 S)-5-Norbornene-2-carboxylic Acid, Incorporating Efficient Recovery of the Chiral Auxiliary d-Pantolactone.
Chang H, et al.
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Controlled Synthesis of Reactive Polymeric Architectures Using 5-Norbornene-2-carboxylic Acid Pentafluorophenyl Ester.
Vogel N and Theato P.
Macromolecular Symposia, 249(1) (2007)
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