Thiomorpholine
Suppliers
Names
[ CAS No. ]:
123-90-0
[ Name ]:
Thiomorpholine
[Synonym ]:
T6M DSTJ
1-Thia-4-azacyclohexane
perhydro-1,4-thiazine
EINECS 204-660-2
Thiomorpholine
UNII-3A8R61G6QV
Tetrahydro-2H-1,4-thiazine,Thiamorpholine
thiamorpholine
Thiazolidinane
parathiazan
1,4-Thiazane
Tetrahydro-2H-1,4-thiazine
[1,4]thiazinane
MFCD00005974
1,4-Thiazan
tetrahydro-1,4-thiazine
Chemical & Physical Properties
[ Density]:
1.0±0.1 g/cm3
[ Boiling Point ]:
170.0±15.0 °C at 760 mmHg
[ Melting Point ]:
166-168
[ Molecular Formula ]:
C4H9NS
[ Molecular Weight ]:
103.19
[ Flash Point ]:
60.0±0.0 °C
[ Exact Mass ]:
103.045570
[ PSA ]:
37.33000
[ LogP ]:
0.27
[ Vapour Pressure ]:
1.5±0.3 mmHg at 25°C
[ Index of Refraction ]:
1.499
MSDS
Safety Information
[ Symbol ]:
GHS05
[ Signal Word ]:
Danger
[ Hazard Statements ]:
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 ]:
C:Corrosive;
[ Risk Phrases ]:
R34;R37
[ Safety Phrases ]:
S26-S36/37/39-S45
[ RIDADR ]:
UN 3267 8/PG 3
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ Hazard Class ]:
8
[ HS Code ]:
2934999090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2934999090
[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Articles
Arch. Pharm. (Weinheim) 347(6) , 415-22, (2014)
A new series of N1-(flavon-6-yl)amidrazones were synthesized by reacting the hydrazonoyl chloride derived from 6-aminoflavone with the appropriate sec-cyclic amines. The antitumor activities of these ...
Bioorg. Med. Chem. 23(9) , 2024-34, (2015)
Recently we described a novel pyranopyridine inhibitor (MBX2319) of RND-type efflux pumps of the Enterobacteriaceae. MBX2319 (3,3-dimethyl-5-cyano-8-morpholino-6-(phenethylthio)-3,4-dihydro-1H-pyrano[...
Org. Lett. 16(13) , 3556-9, (2014)
Secondary amines react with thiosalicylaldehydes in the presence of catalytic amounts of acetic acid to generate ring-fused N,S-acetals in redox-neutral fashion. A broad range of amines undergo α-sulf...