Skip to Content
MilliporeSigma
All Photos(1)

Documents

549940

Sigma-Aldrich

6-Chlorohexanoyl chloride

96%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
Cl(CH2)5COCl
CAS Number:
19347-73-0
Molecular Weight:
169.05
EC Number:
242-979-9
MDL number:
MFCD00041436
UNSPSC Code:
12352100
PubChem Substance ID:
24874734
NACRES:
NA.22

assay

96%

refractive index

n20/D 1.4640 (lit.)

density

1.400 g/mL at 25 °C (lit.)

SMILES string

ClCCCCCC(Cl)=O

InChI

1S/C6H10Cl2O/c7-5-3-1-2-4-6(8)9/h1-5H2

InChI key

WZILXAPNPKMOSA-UHFFFAOYSA-N

Application

6-Chlorohexanoyl chloride may be used in the following processes:
  • Preparation of tert-butyl-N-(2-(6-chlorovaleryl)phenyl)carbamate, an intermediate for synthesizing the ketone analog of 2-amino-N-(4-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)-butyl)benzamide hydrochloride.
  • Preparation of (S)-(-)6-chlorohexanoic acid (2-methoxymethylpyrrolidin-1-yl)amide, a precursor for synthesizing 2-alkyl-substituted lactones.
  • Deprotection and acylation of the pendant nitrogen during the preparation of a new cryptand with hydroxamate moiety that can bind with tribasic cations.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

supp_hazards

EUH014

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

4-Bromobutyric acid 98%

Sigma-Aldrich

258083

4-Bromobutyric acid

Analogues of the potential antipsychotic agent 1192U90: amide modifications.
Navas III F, et al.
Bioorganic & Medicinal Chemistry, 6(6), 811-823 (1998)
Enantioselective Synthesis of 2-Substituted 6-and 7-Membered Lactones via a-Alkylation of Lactone Hydrazones.
Enders D, et al.
Synthesis, 1995(08), 947-951 (1995)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service