W361518

Sigma-Aldrich

Thiazole

≥99%

Empirical Formula (Hill Notation):
C3H3NS
CAS Number:
Molecular Weight:
85.13
FEMA Number:
3615
Beilstein/REAXYS Number:
103852
EC Number:
Council of Europe no.:
11642
MDL number:
PubChem Substance ID:
Flavis number:
15.028
NACRES:
NA.21
Pricing and availability is not currently available.

Quality Level

biological source

synthetic

grade

Halal
Kosher

assay

≥99%

refractive index

n20/D 1.538 (lit.)

bp

117-118 °C (lit.)

density

1.2 g/mL at 25 °C (lit.)

Documentation

see Safety & Documentation for available documents

Featured Industry

Flavors and Fragrances

Organoleptic

nutty

food allergen

no known allergens

SMILES string

c1cscn1

InChI

1S/C3H3NS/c1-2-5-3-4-1/h1-3H

InChI key

FZWLAAWBMGSTSO-UHFFFAOYSA-N

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Related Categories

Packaging

25, 100 g in glass bottle
1 kg in glass bottle

Other Notes

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Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Statements

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Hazard Codes

Xn

Risk Statement

10-22-37/38-41

Safety Statement

16-26-39

RIDADR

UN 1993C 3 / PGIII

WGK Germany

WGK 3

Flash Point(F)

71.6 °F - closed cup

Flash Point(C)

22 °C - closed cup

Yukiko Kiniwa et al.
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Immunotherapy has emerged as a promising strategy for the treatment of metastatic melanoma. Clinical studies have demonstrated the feasibility of cancer immunotherapy using tumor antigens recognized by CD8(+) T cells. However, the overall immune responses induced by these antigens are...
Eita Sasaki et al.
Nature, 510(7505), 427-431 (2014-05-13)
Sulphur is an essential element for life and is ubiquitous in living systems. Yet how the sulphur atom is incorporated into many sulphur-containing secondary metabolites is poorly understood. For bond formation between carbon and sulphur in primary metabolites, the major...
Maria Hayashi et al.
Journal of nutritional science and vitaminology, 61(3), 270-274 (2015-08-01)
The biosynthetic pathways of the thiazole moiety of thiamin were studied in the archaeon Halobacterium salinarum. Thiamin is generated by the union of 4-amino-5-hydroxymethyl-2-methylpyrimidine (pyrimidine) and 5-(2-hydroxyethyl)-4-methylthiazole (thiazole). The biosynthesis of thiazole is different in facultative anaerobes, aerobes and eukaryotes....
Mohammad Sayed Alam et al.
Chemical & pharmaceutical bulletin, 62(12), 1259-1268 (2014-12-03)
A novel series of 2-arylidenehydrazinyl-4-arylthiazole analogues (3a-p) was designed and synthesized in excellent yields using a rapid, simple, efficient methodology. Sixteen novel compounds were screened for in vitro antimicrobial activities against eleven bacteria, namely, Staphylococcus aureus, Listeria monocytogenes, Enterococcus faecalis...
Shruthi Vaidhyanathan et al.
Drug metabolism and disposition: the biological fate of chemicals, 42(8), 1292-1300 (2014-05-31)
Brain metastases are a major cause of mortality in patients with advanced melanoma. Adequate brain distribution of targeted agents for melanoma will be critical for treatment success. Recently, improvement in overall survival led to US Food and Drug Administration (FDA)...

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