4-Methoxyphenylisocyanate

Names

[ Name ]:
4-Methoxyphenylisocyanate

[Synonym ]:
EINECS 226-513-1
4-Methoxyphenylisocyanate
p-Methoxyphenyl isocyanate
4-Methoxyphenyl Isocyanate
MFCD00002026
1-Isocyanato-4-methoxybenzene
4-Isocyanatophenyl methyl ether
Benzene, 1-isocyanato-4-methoxy-
Isocyanic Acid 4-Methoxyphenyl Ester

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
221.5±23.0 °C at 760 mmHg

[ Molecular Formula ]:
C₈H₇NO₂

[ Molecular Weight ]:
149.147

[ Flash Point ]:
98.3±0.0 °C

[ Exact Mass ]:
149.047684

[ PSA ]:
38.66000

[ LogP ]:
2.40

[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.510

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H302 + H312 + H332-H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36/37/39-S45-S37/39

[ RIDADR ]:
UN 2206 6.1/PG 3

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2929109000

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2929109000

[ Summary ]:
2929109000. other isocyanates. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

CO2 and Sn(II) adducts of N-heterocyclic carbenes as delayed-action catalysts for polyurethane synthesis.

Chemistry 15(13) , 3103-9, (2009)

Catalytic rivals: Both CO(2)-protected tetrahydropyrimidin-2-ylidene-based N-heterocyclic carbenes (NHCs) and Sn(II)-1,3-dimesitylimidazol-2-ylidene, as well as Sn(II)-1,3-dimesitylimidazolin-2-yliden...

Biradicals from Thermolysis of N-[2-(1-Alkynyl)phenyl]-N'-phenylcarbodiimides and Their Subsequent Transformations to 6H-Indolo[2,3-b]quinolines.

J. Org. Chem. 64(3) , 925-932, (1999)

Thermolysis of the carbodiimide 9a in gamma-terpinene at 138 degrees C produced 2-(phenylamino)quinoline (11a, 49%) and the parent 6H-indolo[2,3-b]quinoline (14a, 16%). Apparently, 11a was produced vi...

Design, synthesis, and biological evaluation of C9- and C2-substituted pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as new A2A and A3 adenosine receptors antagonists.

J. Med. Chem. 46(7) , 1229-41, (2003)

In the past few years, our group has been involved in the development of A(2A) and A(3) adenosine receptor antagonists which led to the synthesis of SCH58261 (5-amino-7-(2-phenylethyl)-2-(2-furyl)pyra...