4-methoxyphenylisothiocyanate

Names

[ Name ]:
4-methoxyphenylisothiocyanate

[Synonym ]:
4-methoxybenzenisothiocyanate
EINECS 218-921-3
1-isothiocyanato-4-methoxy-benzene
p-Methoxyphenyl isothiocyanate
4-Methoxyphenyl isothiocyanate
Benzene,1-isothiocyanato-4-methoxy
4-methoxyphenylisothiocyanate
MFCD00011676
Benzene, 1-isothiocyanato-4-methoxy-
4-MeOC6H4NCS
4-Isothiocyanatophenyl methyl ether
p-MeOC6H4-NCS
Isothiocyanic Acid 4-Methoxyphenyl Ester
1-Isothiocyanato-4-methoxybenzene

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
280.5±0.0 °C at 760 mmHg

[ Melting Point ]:
18 °C(lit.)

[ Molecular Formula ]:
C₈H₇NOS

[ Molecular Weight ]:
165.212

[ Flash Point ]:
119.5±22.6 °C

[ Exact Mass ]:
165.024841

[ PSA ]:
53.68000

[ LogP ]:
3.59

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.552

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05, GHS08

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314-H317-H334

[ Precautionary Statements ]:
P261-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 ]:
C

[ Risk Phrases ]:
R34:Causes burns. R42:May cause sensitization by inhalation.

[ Safety Phrases ]:
S26-S27-S28-S36-S45

[ RIDADR ]:
UN 1760 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
8

[ HS Code ]:
2930909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Synthesis of some new 1,3,4-thiadiazol-2-ylmethyl-1,2,4-triazole derivatives and investigation of their antimicrobial activities.

Eur. J. Med. Chem. 44 , 2896-903, (2009)

4-Amino-2-[(5-arylamino-4,5-dihydro-1,3,4-thiadiazol-2-yl)methyl]-5-(4-methylphenyl)-2,4-dihydro-3H-1,2,4-triazol-3-ones (3a-c) were obtained in acidic media via the formation of 2-[(4-amino-3-aryl-5-...

Synthesis and antihypertensive activity of novel 3-benzyl-2-substituted-3H-[1,2,4]triazolo[5,1-b]quinazolin-9-ones.

Bioorg. Med. Chem. 15(10) , 3457-62, (2007)

A series of 3-benzyl-2-substituted-3H-[1,2,4]triazolo[5,1-b]quinazolin-9-ones have been synthesized by the cyclocondensation of 3-amino-2-benzylamino-3H-quinazolin-4-one with a variety of one-carbon d...

Development of sensitive radioiodinated anti-sense oligonucleotide probes by conjugation technique.

Bioconjug. Chem. 2(4) , 195-200, (1991)

Radioactive and nonradioactive oligonucleotide (ON) probes have been used in a variety of studies of in vitro hybridization for locations of specific genes and determination of the level of mRNA trans...