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Sigma-Aldrich

6-Bromohexanoyl chloride

97%

Synonym(s):

6-Bromocaproyl chloride, 6-Bromohexanoic acid chloride

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About This Item

Linear Formula:
Br(CH2)5COCl
CAS Number:
Molecular Weight:
213.50
Beilstein/REAXYS Number:
1749739
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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.)

SMILES string

ClC(=O)CCCCCBr

InChI

1S/C6H10BrClO/c7-5-3-1-2-4-6(8)9/h1-5H2

InChI key

HBPVGJGBRWIVSX-UHFFFAOYSA-N

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Related Categories

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

pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

supp_hazards

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

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


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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