推薦產品
形狀
liquid
品質等級
反應適用性
reagent type: oxidant
濃度
2.0 M in methylene chloride
密度
1.335 g/mL at 25 °C
官能基
acyl chloride
SMILES 字串
ClC(=O)C(Cl)=O
InChI
1S/C2Cl2O2/c3-1(5)2(4)6
InChI 密鑰
CTSLXHKWHWQRSH-UHFFFAOYSA-N
尋找類似的產品? 前往 產品比較指南
應用
草酰氯一般用作二甲基亚砜活化剂 和氯化剂,将羧酸转化为酸性氯化物。
訊號詞
Danger
危險分類
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3 - Water-react 1
標靶器官
Central nervous system
儲存類別代碼
4.3 - Hazardous materials which set free flammable gases upon contact with water
水污染物質分類(WGK)
WGK 2
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide" activated" by oxalyl chloride.
The Journal of Organic Chemistry, 43(12), 2480-2482 (1978)
The Journal of organic chemistry, 70(4), 1474-1477 (2005-02-12)
[reaction: see text] Several natural pulvinic acids were synthesized. Silyl ketene acetals derived from methyl arylacetates (4 equiv) reacted with oxalyl chloride at -78 degrees C, without the need of adding a catalyst. After treatment of the crude diketones with
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[reaction: see text] A mild, practical, one-pot method for the generation of imidoyl chlorides and their subsequent in situ reaction with pyridine-1-oxides is described. The imidoyl chlorides were formed from the reaction of secondary amides with a stoichiometric amount of
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