推薦產品
化驗
99%
形狀
liquid
折射率
n20/D 1.546 (lit.)
bp
200 °C (lit.)
密度
1.246 g/mL at 25 °C (lit.)
SMILES 字串
Cc1ccc(Cl)cc1Cl
InChI
1S/C7H6Cl2/c1-5-2-3-6(8)4-7(5)9/h2-4H,1H3
InChI 密鑰
FUNUTBJJKQIVSY-UHFFFAOYSA-N
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應用
2,4-二氯甲苯在使用原位(N-杂环卡宾)-Ni(0)体系的二级醇无氧催化氧化中，可作为氧化剂和溶剂。已用作罗尔斯顿菌(Ralstonia)PS12菌株培养基的生长补充剂。它已用于开发依次采用固相微萃取和气相色谱-串联质谱技术，灵敏分析水体样品中氯甲苯的方法。。
危險聲明
危險分類
Aquatic Chronic 2
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
174.2 °F
閃點（°C）
79 °C
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號，寫有 ‘Lot’或‘Batch’.。
客戶也查看了
[Gas chromatographic determination of 2,4-dichlorotoluene in water].
T A Kozeĭko et al.
Gigiena i sanitariia, (3)(3), 44-45 (1988-03-01)
V Karunakaran et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 95, 64-72 (2012-05-23)
The FT-IR and FT-Raman spectra of α-bromo-2,6-dichlorotoluene (αBDCT) have been recorded. The structural and spectroscopic data of the molecule in the ground state have been calculated using Hartree Fock (HF) and Density Functional Theory (DFT)/B3LYP with the standard 6-31++G(d,p) basis
Omid Khakshoor et al.
Journal of the American Chemical Society, 134(6), 3154-3163 (2012-02-04)
We address the recent debate surrounding the ability of 2,4-difluorotoluene (F), a low-polarity mimic of thymine (T), to form a hydrogen-bonded complex with adenine in DNA. The hydrogen bonding ability of F has been characterized as small to zero in
Christophe Berini et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(23), 6857-6860 (2010-05-11)
The selective, anaerobic catalytic oxidation of secondary alcohols at room temperature by using an in situ (N-heterocyclic carbene)-Ni(0) system is presented. The use of non-anhydrous, non-degassed 2,4-dichlorotoluene as both the oxidant and the solvent allows for very short reaction times
Katrin Pollmann et al.
Journal of bacteriology, 184(19), 5261-5274 (2002-09-10)
Ralstonia sp. strain PS12 is able to use 2,4-, 2,5-, and 3,4-dichlorotoluene as growth substrates. Dichloromethylcatechols are central intermediates that are formed by TecA tetrachlorobenzene dioxygenase-mediated activation at two adjacent unsubstituted carbon atoms followed by TecB chlorobenzene dihydrodiol dehydrogenase-catalyzed rearomatization
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