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238600

Sigma-Aldrich

4-Methoxyphenyl isocyanate

99%

Synonym(s):

1-Isocyanato-4-methoxybenzene, 4-Anisyl isocyanate, 4-Isocyanatoanisole, p-Anisyl isocyanate, p-Methoxyphenyl isocyanate

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About This Item

Linear Formula:
CH3OC6H4NCO
CAS Number:
5416-93-3
Molecular Weight:
149.15
Beilstein:
471920
EC Number:
226-513-1
MDL number:
MFCD00002026
UNSPSC Code:
12352100
PubChem Substance ID:
24854336
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.548 (lit.)

bp

106-110 °C/16 mmHg (lit.)

density

1.151 g/mL at 25 °C (lit.)

functional group

isocyanate

SMILES string

COc1ccc(cc1)N=C=O

InChI

1S/C8H7NO2/c1-11-8-4-2-7(3-5-8)9-6-10/h2-5H,1H3

InChI key

FMDGXCSMDZMDHZ-UHFFFAOYSA-N

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General description

Cyclotrimerization of 4-methoxyphenyl isocyanate by CO2-protected N-heterocyclic carbenes based on tetrahydropyrimidin-2-ylidenes has been reported.

Application

4-Methoxyphenyl isocyanate has been used in the preparation of:
  • 6H-indolo[2,3-b]quinolines
  • 1-[2-(2-furyl)-8-methyl-9-substituted-8H-pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c] pyrimidin-5-yl]-3-(4-methoxyphenyl)urea

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW9224
MKCM5655
MKCH5779
MKCF1394
MKBW1914V

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Geng Li et al.
Chirality, 27(8), 518-522 (2015-06-04)
Ten novel xylan bisphenylcarbamate derivatives bearing meta- and para-substituents on their phenyl groups were synthesized and their chiral recognition abilities were evaluated as the chiral stationary phases (CSPs) for high-performance liquid chromatography (HPLC) after coating them on macroporous silica. The
Pier Giovanni Baraldi et al.
Journal of medicinal chemistry, 46(7), 1229-1241 (2003-03-21)
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)pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine, 61), potent and very selective at the A(2A) receptor subtype, and N(8)-substituted-pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines-N(5)-urea
Bhasker Bantu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(13), 3103-3109 (2009-02-13)
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-ylidene complexes (example displayed), have been identified as truly latent catalysts for polyurethane (PUR) synthesis rivaling all existing systems both in activity and latency.A series of CO(2)-protected
Chongsheng Shi et al.
The Journal of organic chemistry, 64(3), 925-932 (2001-10-25)
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 via the biradical 10a followed by hydrogen-atom abstraction from gamma-terpinene. A two-step biradical pathway through

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