123889
α,α′-二氯-邻-二甲苯
98%
别名:
1,2-双(氯甲基)苯, 邻二甲苯二氯
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关于此项目
线性分子式:
C6H4(CH2Cl)2
化学文摘社编号:
分子量:
175.06
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-291-8
Beilstein/REAXYS Number:
2043675
MDL number:
产品名称
α,α′-二氯-邻-二甲苯, 98%
InChI key
FMGGHNGKHRCJLL-UHFFFAOYSA-N
InChI
1S/C8H8Cl2/c9-5-7-3-1-2-4-8(7)6-10/h1-4H,5-6H2
SMILES string
ClCc1ccccc1CCl
assay
98%
form
solid
bp
239-241 °C (lit.)
mp
51-55 °C (lit.)
functional group
chloro
Quality Level
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Application
α，α′−二氯邻二甲苯用于固相合成基本肽单元的大组合变体。
General description
α，α′-二氯邻二甲苯在2-甲氧基乙醇中与元素碲和NaI反应生成1，1-二碘-3，4-苯并-1-碲尿嘧啶环戊烷。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
257.0 °F - closed cup
flash_point_c
125 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
William L Scott et al.
Molecules (Basel, Switzerland), 15(7), 4961-4983 (2010-07-27)
Amino acids are Nature's combinatorial building blocks. When substituted on both the amino and carboxyl sides they become the basic scaffold present in all peptides and proteins. We report a solid-phase synthetic route to large combinatorial variations of this fundamental
The synthesis and characterization of α-and β-1, 1-diiodo-3, 4-benzo-1-telluracyclopentane, C8 H8Tel2.
Ziolo RF and Gunther WHH.
Journal of Organometallic Chemistry, 146(3), 245-251 (1978)
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