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线性分子式:
CH3CH2CH2COCl
化学文摘社编号:
分子量:
106.55
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-498-5
Beilstein/REAXYS Number:
605395
MDL number:
产品名称
丁酰氯, ≥99%
InChI key
DVECBJCOGJRVPX-UHFFFAOYSA-N
InChI
1S/C4H7ClO/c1-2-3-4(5)6/h2-3H2,1H3
SMILES string
CCCC(Cl)=O
vapor density
3.7 (vs air)
assay
≥99%
form
liquid
refractive index
n20/D 1.412 (lit.)
bp
102 °C (lit.)
mp
−89 °C (lit.)
solubility
diethyl ether: miscible(lit.)
density
1.026 g/mL at 25 °C (lit.)
functional group
acyl chloride
Quality Level
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Application
Butyryl chloride can be used as:
- A reagent in the acylation of thiophene in the liquid phase catalyzed by zeolites.
- A source of CO and -Cl in the chlorocarbonylation of aryl bromides to yield acid chlorides.
- An intermediate in the synthesis of aryl [11C]methylsulfones for PET applications.
General description
Photchlorination of butyryl chloride in liquid phase has been investigated.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
64.4 °F - DIN 51755 Part 1
flash_point_c
18 °C - DIN 51755 Part 1
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
A lewis acid site-activated reaction in zeolites: thiophene acylation by butyryl chloride.
Isaev Y and Fripiat JJ.
J. Catal., 182(1), 257-263 (1999)
Palladium-catalyzed Chlorocarbonylation of Aryl (pseudo) Halides through in situ Generation of Carbon Monoxide
Boehm P, et al.
Angewandte Chemie (International Edition in English), 132(41), 18043-18052 (2020)
CHLORINATION OF BUTYRYL CHLORIDE IN THE LIQUID-PHASE.
Korhonen IO.
Acta Chemica Scandinavica. Series B, 35(3), 175-178 (1981)
A Lewis acid site-activated reaction in zeolites: Thiophene acylation by butyryl chloride
Isaev Y and Fripiat JJ
J. Catal., 182(1), 257-263 (1999)
A general method for the synthesis of aryl [11C] methylsulfones: potential PET probes for imaging cyclooxygenase-2 expression
Majo VJ, et al.
Bioorganic & Medicinal Chemistry Letters, 15(19), 4268-4271 (2005)
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