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88345

Sigma-Aldrich

Thiomorpholine hydrochloride

≥98.0% (AT)

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About This Item

Empirical Formula (Hill Notation):
C4H9NS · HCl
CAS Number:
5967-90-8
Molecular Weight:
139.65
Beilstein:
3908104
EC Number:
227-757-1
MDL number:
MFCD00043266
UNSPSC Code:
12352100
PubChem Substance ID:
57653301
NACRES:
NA.22

Assay

≥98.0% (AT)

form

crystals

mp

174-177 °C

storage temp.

2-8°C

SMILES string

Cl[H].C1CSCCN1

InChI

1S/C4H9NS.ClH/c1-3-6-4-2-5-1;/h5H,1-4H2;1H

InChI key

QSJAHJYXDRUZMY-UHFFFAOYSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

88345-VAR:
88345-BULK:
88345-5G:

Certificates of Analysis (COA)

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I T Ermakova et al.
Mikrobiologiia, 77(5), 617-622 (2008-11-14)
A screening of lignin-degrading basidial fungi that can grow in the presence of thiomorpholine derivatives (the mixture of 1,4-perhydrothiazines) has been performed. Strain Bjerkandera adusta VKM F-3477 was shown to have the maximal rate of growth in the presence of
Saurav Bera et al.
ACS combinatorial science, 14(1), 1-4 (2011-12-01)
Diastereoselective trans-2,5-disubstituted amino acids derived diverse morpholines, piperazines and thiomorpholines were prepared in 30 min-1 h with high yields through iodine-mediated 6-exotrig type cyclization from a single common synthetic intermediate. The displacement of iodine with hydride ion gave a methyl
B Combourieu et al.
Biodegradation, 9(6), 433-442 (1999-05-21)
Spectrophotometric assays of Mycobacterium aurum MO1 cells extracts gave evidence of a soluble cytochrome P450, involved in the degradative pathway of morpholine, a waste product from the chemical industry. In order to get further information, the kinetics of the biodegradation
B Beck et al.
Molecular diversity, 14(3), 479-491 (2010-04-22)
We designed two novel thiolactone scaffolds. Both scaffolds can be accessed by a convergent Ugi multicomponent reaction (MCR) and are, thus, amenable to library synthesis. Design, stereoselectivity, structures, full experimental details, and virtual libraries will be reported.
Javad Mirzaei et al.
European journal of medicinal chemistry, 43(8), 1575-1580 (2008-01-15)
Synthesis and in vitro anti-Helicobacter pylori activity of N-[5-(5-nitro-2-heteroaryl)-1,3,4-thiadiazol-2-yl]thiomorpholines 5-7(a-c) and some related compounds 8a-c and 9a-c were described. The anti-H. pylori activity of target compounds along with commercially available antibiotics such as metronidazole and amoxicillin was evaluated by comparing
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