Skip to Content
MilliporeSigma
All Photos(1)

Documents

159360

Sigma-Aldrich

3-Fluorophenyl isocyanate

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
FC6H4NCO
CAS Number:
Molecular Weight:
137.11
Beilstein/REAXYS Number:
774879
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.514 (lit.)

density

1.201 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

Fc1cccc(c1)N=C=O

InChI

1S/C7H4FNO/c8-6-2-1-3-7(4-6)9-5-10/h1-4H

InChI key

RIKWVZGZRYDACA-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

3-Fluorophenyl isocyanate is an aryl fluorinated building block used in chemical synthesis.

Application

3-Fluorophenyl isocyanate was used in the synthesis of linezolid. It was also used in the preparation of substituted 6-ureidopurines, 6(N2-3-fluorophenyl)ureidopurine.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

107.6 °F - closed cup

flash_point_c

42 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

New synthetic method of linezolid.
Yu D-S, et al.
Chinese Journal of Medicinal Chemistry / Zhong Guo Yao Wu Hua Xue Za Zhi, 2, 2-2 (2005)
Synthesis of new substituted 6-ureidopurines and 6-ureido-9-(2, 3, 5-triacetylribofuranosyl) purines having cytokinin (plant growth promoting) activity.
Mhatre V and Joshi V.
Indian J. Chem. B, 41(12), 2667-2675 (2002)

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