W361518
噻唑
≥99%
别名:
1,3-thiazole
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关于此项目
经验公式（希尔记法）:
C3H3NS
化学文摘社编号:
分子量:
85.13
FEMA编号:
3615
Beilstein:
103852
EC 号:
欧洲委员会编号:
11642
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
15.028
NACRES:
NA.21
Agency:
meets purity specifications of JECFA
生物来源
synthetic
等级
Halal
Kosher
Agency
meets purity specifications of JECFA
方案
≥99%
折射率
n20/D 1.538 (lit.)
沸点
117-118 °C (lit.)
密度
1.2 g/mL at 25 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens
性状检查
nutty
SMILES字符串
c1cscn1
InChI
1S/C3H3NS/c1-2-5-3-4-1/h1-3H
InChI key
FZWLAAWBMGSTSO-UHFFFAOYSA-N
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免责声明
For R&D or non-EU Food use. Not for retail sale.
警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Flam. Liq. 2
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
71.6 °F - closed cup
闪点(°C)
22 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
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
Yukiko Kiniwa et al.
PloS one, 10(5), e0124094-e0124094 (2015-05-21)
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
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
Zhiyang Jia
OncoTargets and therapy, 8, 1561-1565 (2015-07-08)
The objective of the present investigation was to investigate the role of integrin-linked kinase (ILK) in the gemcitabine-resistant lung cancer cell line A549 and explore the underlying mechanism. Gemcitabine-resistant A549 (A549/GemR) cell line was established by pulse-exposed to moderate concentration
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