Thiomorpholine structure
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Common Name | Thiomorpholine | ||
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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 |
Signal Word | Danger |
Use of ThiomorpholineThiomorpholine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | thiomorpholine |
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Synonym | More Synonyms |
Description | Thiomorpholine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog |
Density | 1.0±0.1 g/cm3 |
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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 |
Symbol |
GHS05 |
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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 |
~% Thiomorpholine CAS#:123-90-0 |
Literature: Journal of the American Chemical Society, , vol. 76, p. 1187 |
~% Thiomorpholine CAS#:123-90-0 |
Literature: Chemical and Pharmaceutical Bulletin, , vol. 57, # 12 p. 1415 - 1420 |
~% Thiomorpholine CAS#:123-90-0 |
Literature: Journal of the Chemical Society, , vol. 117, p. 299 |
~% Thiomorpholine CAS#:123-90-0 |
Literature: Journal of Organic Chemistry, , vol. 73, # 18 p. 7189 - 7196 |
~% Thiomorpholine CAS#:123-90-0 |
Literature: Australian Journal of Chemistry, , vol. 9, p. 397,402 Chim. moderne, , vol. 4, p. 53 - 55 |
~% Thiomorpholine CAS#:123-90-0 |
Literature: Bihang till Svenska Vet.-Akad. Handlingar 22 II, No. 1, S. 5 |
~% Thiomorpholine CAS#:123-90-0 |
Literature: Australian Journal of Chemistry, , vol. 9, p. 397,402 |
~% Thiomorpholine CAS#:123-90-0 |
Literature: Bihang till Svenska Vet.-Akad.Handlingar, vol. 22, p. II,No.1,S.5 |
Precursor 7 | |
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DownStream 9 | |
HS Code | 2934999090 |
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Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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 ... |
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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[... |
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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... |
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 |