273449
(4R)-(-)-2-硫酮基-4-噻唑烷羧酸
99%
别名:
(R)-(-)-2-硫酮基-4-噻唑烷羧酸, Raphanusamic acid
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关于此项目
经验公式（希尔记法）:
C4H5NO2S2
CAS Number:
分子量:
163.22
Beilstein:
82632
MDL编号:
UNSPSC代码:
12352202
PubChem化学物质编号:
NACRES:
NA.22
方案
99%
表单
powder
旋光性
[α]29/D −86°, c = 2.5 in 0.5 M HCl
反应适用性
reaction type: solution phase peptide synthesis
mp
179-181 °C (lit.)
应用
peptide synthesis
SMILES字符串
OC(=O)[C@@H]1CSC(=S)N1
InChI
1S/C4H5NO2S2/c6-3(7)2-1-9-4(8)5-2/h2H,1H2,(H,5,8)(H,6,7)/t2-/m0/s1
InChI key
SQUOCHQOQMZGQP-REOHCLBHSA-N
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
S E Sparks et al.
Journal of biochemical and molecular toxicology, 14(1), 26-32 (1999-11-24)
Chloropicrin (CCl3NO2) is a widely used soil fumigant with an unknown mechanism of acute toxicity. We investigated the possible involvement of dechlorination in CCl3NO2 toxicity by considering its metabolism, inhibition of pyruvate and succinate dehydrogenases, cytotoxicity in cultured cells, and
A J Dobson et al.
Acta crystallographica. Section C, Crystal structure communications, 54 ( Pt 11), 1634-1637 (1998-12-19)
The title acid, C4H5NO2S2, crystallized in the noncentrosymmetric space group P2(1)2(1)2(1) with one molecule as the asymmetric unit. Two hydrogen bonds occur, namely, N--H...O, with a donor-acceptor distance of 2.850 (2) A, and O-H...S (resonance induced), with a donor-acceptor distance
A glucosinolate metabolism pathway in living plant cells mediates broad-spectrum antifungal defense.
Pawel Bednarek et al.
Science (New York, N.Y.), 323(5910), 101-106 (2008-12-20)
Selection pressure exerted by insects and microorganisms shapes the diversity of plant secondary metabolites. We identified a metabolic pathway for glucosinolates, known insect deterrents, that differs from the pathway activated by chewing insects. This pathway is active in living plant
V Amarnath et al.
Chemical research in toxicology, 14(9), 1277-1283 (2001-09-18)
A new method is reported for the analysis of 2-thioxothiazolidine-4-carboxylic acid (TTCA) in urine that is amenable to automation and provides greatly simplified chromatograms. The method comprises the addition of tetrahydro-2-thioxo-2H-1,3-thiazine-4-carboxylic acid, which is chemically similar to TTCA, as internal
Verena Jeschke et al.
Frontiers in plant science, 10, 1560-1560 (2019-12-24)
Dynamically changing environmental conditions promote a complex regulation of plant metabolism and balanced resource investments to development and defense. Plants of the Brassicales order constitutively allocate carbon, nitrogen, and sulfur to synthesize glucosinolates as their primary defense metabolites. Previous findings
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