235555
6-溴己酰氯
97%
别名:
6-Bromocaproyl chloride, 6-Bromohexanoic acid chloride
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关于此项目
线性分子式:
Br(CH2)5COCl
化学文摘社编号:
分子量:
213.50
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
245-236-7
Beilstein/REAXYS Number:
1749739
MDL number:
Assay:
97%
Form:
liquid
InChI key
HBPVGJGBRWIVSX-UHFFFAOYSA-N
InChI
1S/C6H10BrClO/c7-5-3-1-2-4-6(8)9/h1-5H2
SMILES string
ClC(=O)CCCCCBr
assay
97%
form
liquid
refractive index
n20/D 1.486 (lit.)
bp
130 °C/20 mmHg (lit.)
density
1.395 g/mL at 25 °C (lit.)
functional group
acyl chloride, bromo
Quality Level
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Application
6-Bromohexanoyl chloride has been used in preparation of:
- (S)- or (R)-N-(6-bromohexanoyl)-α-methylbenzylamine
- 1-bromoheptadecan-6-one and 1-bromooctadecan-6-one
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
supp_hazards
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
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An enantiomeric discrimination in aqueous mixed chiral micelles through hydrogen bonding.
Jursic BS.
Tetrahedron Letters, 34(6), 963-966 (1993)
Tomás Holas et al.
Bioorganic & medicinal chemistry, 14(9), 2896-2903 (2005-12-27)
Transkarbam 12 (5-(dodecyloxycarbonyl)pentylammonium-5-(dodecyloxycarbonyl)pentylcarbamate, T12) is a highly active transdermal permeation enhancer. In this study, ketone, amide, and alkane analogs of T12 have been synthesized and evaluated for their permeation-enhancing activity using porcine skin and theophylline as a model drug. Replacement
Tae Yang Son et al.
Polymers, 12(11) (2020-11-27)
In this study, novel crosslinked pore-filling membranes were fabricated by using a centrifugal force from the cylindrical centrifugal machine. For preparing these crosslinked pore-filling membranes, the poly(phenylene oxide) containing long side chains to improve the water management (hydrophilic), porous polyethylene
Ji Eon Chae et al.
Polymers, 13(5) (2021-03-07)
Polystyrene-based polymers with variable molecular weights are prepared by radical polymerization of styrene. Polystyrene is grafted with bromo-alkyl chains of different lengths through Friedel-Crafts acylation and quaternized to afford a series of hydroxide-ion-conducting ionomers for the catalyst binder for the
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