추천 제품
분석
95%
refractive index
n20/D 1.481 (lit.)
bp
102 °C/16 mmHg (lit.)
203-208 °C (lit.)
mp
10-14 °C (lit.)
density
1.196 g/mL at 25 °C (lit.)
SMILES string
CC(S)C(O)=O
InChI
1S/C3H6O2S/c1-2(6)3(4)5/h2,6H,1H3,(H,4,5)
InChI key
PMNLUUOXGOOLSP-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Thiolactic acid (TLA) can be used as a building block in the synthesis of:
It can also be used as a bidental chelating agent for the surface modification of titanium dioxide (TiO2) nanoparticles for the removal of cadmium from waste water.
- Thiolactomycin via oxathiolanone intermediate.
- 4-Thiazolidinones by reacting various Schiff bases with thioglycolic acid.
- 1,4-Naphthoquinone derivatives containing sulfur atom for antibacterial and antiviral activity studies.
It can also be used as a bidental chelating agent for the surface modification of titanium dioxide (TiO2) nanoparticles for the removal of cadmium from waste water.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Skin Corr. 1B
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 1
Flash Point (°F)
190.4 °F - closed cup
Flash Point (°C)
88 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Synthesis of novel heterocyclic 4-thiazolidinone derivatives and their antibacterial activity
Mistry KM and Desai KR
Journal of Chemistry, 1(4), 189-193 (2004)
A Flexible Route to (5 R)-Thiolactomycin, a Naturally Occurring Inhibitor of Fatty Acid Synthesis
McFadden JM, et al.
Organic Letters, 4(22), 3859-3862 (2002)
Cadmium removal from water using thiolactic acid-modified titanium dioxide nanoparticles
Skubal LR, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 148(1-3), 393-397 (2002)
Synthesis and biological evaluation of novel 1, 4-naphthoquinone derivatives as antibacterial and antiviral agents
Tandon VK, et al.
Bioorganic & Medicinal Chemistry Letters, 15(14), 3463-3466 (2005)
Yunbo Jiang et al.
Chemical communications (Cambridge, England), (44)(44), 6828-6830 (2009-11-04)
Addition of O(2)(g) at low-temperature to a mononuclear, nonheme iron(ii) complex comprising a tetraazamacrocyclic N(4) donor and an arylthiolate S donor leads to the generation of a deep red complex assigned as a low-spin Fe(III)?OOH complex, formed via metal- and
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