모든 사진(2)
About This Item
Linear Formula:
Cl2C6H3NCO
CAS Number:
Molecular Weight:
188.01
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
![1,8-Diazabicyclo[5.4.0]undec-7-ene 98%](/deepweb/assets/sigmaaldrich/product/structures/120/564/5b373e23-1624-489c-8efb-692de0f96ffb/640/5b373e23-1624-489c-8efb-692de0f96ffb.png)
분석
96%
양식
solid
mp
32-34 °C (lit.)
density
1.38 g/mL at 25 °C (lit.)
작용기
chloro
isocyanate
SMILES string
Clc1cc(Cl)cc(c1)N=C=O
InChI
1S/C7H3Cl2NO/c8-5-1-6(9)3-7(2-5)10-4-11/h1-3H
InChI key
XEFUJGURFLOFAN-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
3,5-Dichlorophenyl isocyanate can be used:
- As a reactant to synthesize 3-(3,5-Dichlorophenyl)-2,4-oxazolidinedione (DCPO).
- To synthesize phenylcarbamate derivatives of cellulose and amylose, which are useful as polysaccharide-based chiral stationary phases (CSPs).{70]
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 1 Inhalation - Aquatic Chronic 2 - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1A - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point (°F)
235.4 °F - closed cup
Flash Point (°C)
113 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Synthesis and chiral recognition of amylose derivatives bearing regioselective phenylcarbamate substituents at 2, 6-and 3-positions for high-performance liquid chromatography.
Shen J, et al.
Journal of Chromatography A, 1467, 199-205 (2016)
Synthesis of regioselectively substituted cellulose derivatives and applications in chiral chromatography.
Acemoglu M, et al.
Chirality, 10(4), 294-306 (1998)
Nephrotoxic and hepatotoxic potential of imidazolidinedione-, oxazolidinedione-and thiazolidinedione-containing analogues of N-(3, 5-dichlorophenyl) succinimide (NDPS) in Fischer 344 rats.
Kennedy E, et al.
Toxicology, 186(1-2), 79-91 (2003)
Polymer?bound cellulose phenylcarbamate derivatives as chiral stationary phases for enantioselective HPLC.
Ling F, et al.
Journal of Separation Science, 26(15?16), 1337-1346 (2003)
Alyssa M Keil et al.
Toxicology in vitro : an international journal published in association with BIBRA, 29(7), 1887-1896 (2015-07-21)
Liver damage occurred in some patients who took troglitazone (TGZ) for type II diabetes. The 2,4-thiazolidinedione (TZD) ring in TGZ's structure has been implicated in its hepatotoxicity. To further examine the potential role of a TZD ring in toxicity we
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