149691
Thiazolidine
95%
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About This Item
Empirical Formula (Hill Notation):
C3H7NS
CAS Number:
Molecular Weight:
89.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
95%
form
liquid
refractive index
n20/D 1.5508 (lit.)
bp
72-75 °C/25 mmHg (lit.)
density
1.131 g/mL at 25 °C (lit.)
functional group
thioether
SMILES string
C1CSCN1
InChI
1S/C3H7NS/c1-2-5-3-4-1/h4H,1-3H2
InChI key
OGYGFUAIIOPWQD-UHFFFAOYSA-N
Application
Thiazolidine was used in the synthesis of homogeneous penicillamine disulphide cross-linked polypeptides.
Signal Word
Warning
Hazard Statements
Hazard Classifications
Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
132.8 °F - closed cup
Flash Point(C)
56 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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Takahiro Sawada et al.
Journal of atherosclerosis and thrombosis, 27(7), 644-656 (2019-10-22)
So far, the mechanisms behind the cardiovascular benefits of sodium/glucose cotransporter 2 (SGLT2) inhibitors have not been fully clarified. In order to evaluate the effects of SGLT2 inhibitors on systemic hemodynamics, glucose metabolism, lipid profile, and endothelial function, 50 diabetic
Mark D Ericson et al.
Tetrahedron letters, 54(26), doi:10-doi:10 (2013-12-19)
The syntheses of homogeneous penicillamine disulfide cross-linked polypeptides are reported. Dodecapeptides containing N-terminal, C-terminal, or N- and C-terminal Pen were serially ligated into 36 amino acid polypeptides linked through Cys-Pen, Pen-Cys or Pen-Pen disulfide bonds. Critical to the syntheses was
David Pertuit et al.
Natural product communications, 10(6), 1005-1007 (2015-07-23)
A new aromatic compound 3,4,5-trimethoxyphenyl-1-O-(4-sulfo)-β-D-glucopyranoside (1), in addition to two triterpenoid saponins (chebuloside II, arjunoglucoside II), two triterpenes (arjunolic acid and 3-betulinic acid) and sitosterol-3-O-β-D-glucopyranoside have been isolated from the barks of Terminalia catappa. Their structures have been established on
Sinem Aslan Erdem et al.
Phytochemistry, 110, 160-165 (2014-12-20)
Four new oleanane-type saponins 3-O-α-L-rhamnopyranosyl-(1 → 4)-β-D-glucuronopyranosyl-22-O-β,β-dimethylacryloylA1-barrigenol (1), 3-O-α-L-rhamnopyranosyl-(1 → 4)-β-D-glucuronopyranosyl-22-O-angeloylA1-barrigenol (2), 3-O-β-D-glucopyranosyl-(1 → 2)-[β-D-glucopyranosyl-(1 → 6)]-β-D-glucopyranosyl-21,22,28-O-triacetyl-(3β,21β,22α)-olean-12-en-16-one (3), and 3-O-β-D-glucopyranosyl-(1 → 2)-glucopyranosyl-22-O-β-D-glucopyranosylsteganogenin (4), along with the known 3-O-β-D-galactopyranosyl-(1 → 2)-[α-L-arabinopyranosyl-(1 → 3)]-β-D-glucuronopyranosyl-22-O-angeloylA1-barrigenol and 3-O-α-L-rhamnopyranosyl-(1 → 4)-β-D-glucuronopyranosyloleanolic acid, were isolated from
Structural analysis of oleanane-type saponins from the roots of Wisteria frutescens.
Anne-Sophie Champy et al.
Magnetic resonance in chemistry : MRC, 55(6), 595-600 (2016-11-20)
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