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6-Bromohexanoyl chloride, 97%, Thermo Scientific Chemicals
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Catalog number A11063.14
also known as A11063-14
Price (USD)/ Each
86.40
-
Quantity:
25 g
Price (USD)/ Each
86.40
6-Bromohexanoyl chloride, 97%, Thermo Scientific Chemicals
Catalog numberA11063.14
Price (USD)/ Each
86.40
-
Chemical Identifiers
CAS22809-37-6
IUPAC Name6-bromohexanoyl chloride
Molecular FormulaC6H10BrClO
InChI KeyHBPVGJGBRWIVSX-UHFFFAOYSA-N
SMILESClC(=O)CCCCCBr
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless
Refractive Index1.4850-1.4900 @ 20?C
Assay (GC)≥96.0%
FormLiquid
6-Bromohexanoyl chloride is used as intermediates, organic synthesis, chemical research, agrochemicals and dyestuff.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
6-Bromohexanoyl chloride is used as intermediates, organic synthesis, chemical research, agrochemicals and dyestuff.
Solubility
Reacts with water.
Notes
Store in cool, dry conditions in well sealed containers. Keep container tightly closed. Moisture Sensitive
6-Bromohexanoyl chloride is used as intermediates, organic synthesis, chemical research, agrochemicals and dyestuff.
Solubility
Reacts with water.
Notes
Store in cool, dry conditions in well sealed containers. Keep container tightly closed. Moisture Sensitive
RUO – Research Use Only
General References:
- Koji Matsuoka,; Mikiko Terabatake,; Yosuke Saito,; Chiharu Hagihara,; Yasuaki Esumi,; Daiyo Terunuma. Hiroyoshi Kuzuhara. Synthesis of Carbosilane Compounds Functionalized with Three or Four β-Cyclodextrin Moieties. Use of a One-Pot Reaction in Liquid Ammonia for Birch Reduction and the Subsequent SN2 Replacement. Bulletin of the Chemical Society of Japan. 1998, 71(11),2709-2713.
- Yukito Murakami,; Akio Nakano,; Hidetsugu Ikeda.;Preparation of stable single-compartment vesicles with cationic and zwitterionic amphiphiles involving amino acid residues. J. Org. Chem. 1982, 47(11),2137-2144.