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389056

Sigma-Aldrich

3,5-二氯苯异氰酸酯

96%

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About This Item

線性公式:
Cl2C6H3NCO
CAS號碼:
34893-92-0
分子量：:
188.01
EC號碼:
252-276-9
MDL號碼:
MFCD00013859
分類程式碼代碼:
12352100
PubChem物質ID:
24864259
NACRES:
NA.22

化驗

96%

形狀

solid

mp

32-34 °C (lit.)

密度

1.38 g/mL at 25 °C (lit.)

官能基

chloro
isocyanate

SMILES 字串

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 密鑰

XEFUJGURFLOFAN-UHFFFAOYSA-N

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相關類別

應用

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]

訊號詞

Danger

危險分類

Acute Tox. 1 Inhalation - Aquatic Chronic 2 - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1A - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

水污染物質分類（WGK）

WGK 3

閃點（°F）

235.4 °F - closed cup

閃點（°C）

113 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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分析證明 (COA)

Lot/Batch Number
MKCB1990V
MKBZ5383V
MKBX4776V
MKBW9478V
MKBW8113V

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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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