蒸汽密度
3.2 (vs air)
质量水平
方案
98%
折射率
n20/D 1.404 (lit.)
沸点
77-79 °C (lit.)
mp
−94 °C
密度
1.059 g/mL at 25 °C (lit.)
SMILES字符串
CCC(Cl)=O
InChI
1S/C3H5ClO/c1-2-3(4)5/h2H2,1H3
InChI key
RZWZRACFZGVKFM-UHFFFAOYSA-N
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一般描述
丙酰氯是一种重要化学中间体，用于合成各种丙酸衍生物。。
应用
丙酰氯可用作以下反应的酰化剂：
此外，还可用于：
- 在氯化铟(InCl3)浸染的介孔Si-MCM-41催化剂作用下，将苯甲醚转化为4-间甲氧基苯丙酮以及2-甲氧基萘转化为1-丙氧基-2-甲氧基萘。
此外，还可用于：
- 在存在硫酰氯和过氧化物的条件下氯化，形成α-氯丙酰氯和β-氯丙酰氯。
- 与（羟丙基）纤维素反应生成丙酸酯、[(丙酰氧基)丙基]纤维素。
警示用语：
Danger
危险分类
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
补充剂危害
储存分类代码
3 - Flammable liquids
WGK
WGK 1
闪点(°F)
42.8 °F - closed cup
闪点(°C)
6 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Chlorinations with Sulfuryl Chloride. III.(a) The Peroxide-Catalyzed Chlorination of Aliphatic Acids and Acid Chlorides.(b) The Photochemical Sulfonation of Aliphatic Acids
Kharasch MS and Brown HC
Journal of the American Chemical Society, 62(4), 925-929 (1940)
The propanoate ester of (2-hydroxypropyl) cellulose: a thermotropic cholesteric polymer that reflects visible light at ambient temperatures
Tseng SL, et L.
Macromolecules, 15(5), 1262-1264 (1982)
Acylation of aromatic compounds using moisture insensitive InCl3 impregnated mesoporous Si-MCM-41 catalyst
Choudhary VR, et al.
Tetrahedron Letters, 43(6), 1105-1107 (2002)
Joanna Kurczewska et al.
International journal of pharmaceutics, 486(1-2), 226-231 (2015-04-07)
Vancomycin was immobilized on three different organically functionalized silicas. The materials obtained were used for a controlled release of the antibiotic. The influence of the type of chemical bond on the in vitro drug release was investigated. A weak ionic
Yu Duan et al.
Molecular medicine reports, 16(6), 9735-9740 (2017-10-19)
The aim of the present study was to report on a complete synthetic approach, namely benzylation-hydrolysis-acylation‑hydrogenation, to the synthesis of regioselectively acylated quercetin analogues using low‑cost rutin as a starting material. Three quercetin analogues, quercetin‑3‑O‑propionate (Q‑pr), quercetin‑3‑O‑butyrate (Q‑bu) and quercetin‑3‑O‑valerate
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