Thiomorpholine

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

Biological Activity

[Description]:

Thiomorpholine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

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

Click to get detail 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

Click to get detail 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

Synthesis and antitumor activities of some new N1-(flavon-6-yl)amidrazone derivatives.

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 ...

Structure-activity relationships of a novel pyranopyridine series of Gram-negative bacterial efflux pump inhibitors.

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[...

Redox-neutral α-sulfenylation of secondary amines: ring-fused N,S-acetals.

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...