Thiomorpholine

Modify Date: 2024-01-02 17:25:25

Thiomorpholine Structure
Thiomorpholine structure
Common Name Thiomorpholine
CAS Number 123-90-0 Molecular Weight 103.19
Density 1.0±0.1 g/cm3 Boiling Point 170.0±15.0 °C at 760 mmHg
Molecular Formula C4H9NS Melting Point 166-168
MSDS Chinese USA Flash Point 60.0±0.0 °C
Symbol GHS05
GHS05
Signal Word Danger

 Use of Thiomorpholine


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

 Names

Name thiomorpholine
Synonym More Synonyms

 Thiomorpholine 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

 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

 Safety Information

Symbol GHS05
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

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Thiomorpholine Structure

Thiomorpholine

CAS#:123-90-0

Literature: Journal of the American Chemical Society, , vol. 76, p. 1187

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Thiomorpholine Structure

Thiomorpholine

CAS#:123-90-0

Literature: Chemical and Pharmaceutical Bulletin, , vol. 57, # 12 p. 1415 - 1420

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Thiomorpholine Structure

Thiomorpholine

CAS#:123-90-0

Literature: Journal of the Chemical Society, , vol. 117, p. 299

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Thiomorpholine Structure

Thiomorpholine

CAS#:123-90-0

Literature: Journal of Organic Chemistry, , vol. 73, # 18 p. 7189 - 7196

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Thiomorpholine Structure

Thiomorpholine

CAS#:123-90-0

Literature: Australian Journal of Chemistry, , vol. 9, p. 397,402 Chim. moderne, , vol. 4, p. 53 - 55

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Thiomorpholine Structure

Thiomorpholine

CAS#:123-90-0

Literature: Bihang till Svenska Vet.-Akad. Handlingar 22 II, No. 1, S. 5

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Thiomorpholine Structure

Thiomorpholine

CAS#:123-90-0

Literature: Australian Journal of Chemistry, , vol. 9, p. 397,402

~%

Thiomorpholine Structure

Thiomorpholine

CAS#:123-90-0

Literature: Bihang till Svenska Vet.-Akad.Handlingar, vol. 22, p. II,No.1,S.5

 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%

 Articles22

More 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...

 Synonyms

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
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