All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C11H7ClO2
CAS Number:
Molecular Weight:
206.63
Beilstein:
512216
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
Quality Level
Assay
≥98.0% (GC)
refractive index
n20/D 1.598
density
1.273 g/mL at 20 °C (lit.)
storage temp.
2-8°C
SMILES string
ClC(=O)Oc1cccc2ccccc12
InChI
1S/C11H7ClO2/c12-11(13)14-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H
InChI key
JRUFQZPDRRGHEF-UHFFFAOYSA-N
Application
1-Naphthyl chloroformate was used in preparation of:
- 4-benzyl-2-(4-methoxyphenyl)oxazol-5-yl naphthalen-1-ylcarbonate
- naphthalen-1-yl 4-benzyl-2-(4-methoxyphenyl)-5-oxo-4,5-dihydrooxazole-4-carboxylate
- 2-(4-methoxyphenyl)-4-methyloxazol-5-yl naphthalen-1-ylcarbonate
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 2
Flash Point(F)
257.0 °F - closed cup
Flash Point(C)
125 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Lot/Batch Number
Don't see the Right Version?
If you require a particular version, you can look up a specific certificate by the Lot or Batch number.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Craig D Campbell et al.
Organic & biomolecular chemistry, 9(11), 4205-4218 (2011-04-21)
The O- to C-carboxyl transfer of oxazolyl carbonates promoted by triazolinylidenes, generated in situ with NEt(3), shows a markedly different rate and chemoselectivity profile to the same reaction promoted by triazolinylidenes generated using KHMDS. The mechanism of these pathways has
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service