Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

218111

Sigma-Aldrich

2-Chloro-6-fluorobenzyl chloride

98%

Synonym(s):

2,α-Dichloro-6-fluorotoluene

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

About This Item

Linear Formula:
ClC6H3(F)CH2Cl
CAS Number:
55117-15-2
Molecular Weight:
179.02
EC Number:
259-487-5
MDL number:
MFCD00000896
UNSPSC Code:
12352100
PubChem Substance ID:
24853046
NACRES:
NA.22
Pricing and availability is not currently available.

Assay

98%

form

liquid

refractive index

n20/D 1.537 (lit.)

density

1.401 g/mL at 25 °C (lit.)

functional group

chloro
fluoro

SMILES string

Fc1cccc(Cl)c1CCl

InChI

1S/C7H5Cl2F/c8-4-5-6(9)2-1-3-7(5)10/h1-3H,4H2

InChI key

MJGOLNNLNQQIHR-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

2-Chloro-6-fluorobenzyl chloride was used:
  • as alkylating reagent during the synthesis of 3-benzylsulfanyl derivatives of 1,2,4-triazole and 4-methyl-1,2,4-triazole[1]
  • in the preparataion of 2-chloro-6-fluorobenzylamine, required for the synthesis of 9-substituted adenine[2]
  • in the preparation of aprinocid via reaction with adenine[3]

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

200.1 °F - closed cup

Flash Point(C)

93.4 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBJ3947
STBF1843V
STBB2897V
STBB2897
S15881

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Vera Klimesová et al.
Farmaco (Societa chimica italiana : 1989), 59(4), 279-288 (2004-04-15)
Series of 3-benzylsulfanyl derivatives of 1,2,4-triazole and 4-methyl-1,2,4-triazole were synthesized by alkylation of starting triazole-3-thiol with appropriately substituted benzyl halide. All members of the set were evaluated for in vitro antimycobacterial activity against Mycobacterium tuberculosis, M. avium, and two strains
New synthesis of a 9-substituted adenine.
Hartman GD, et al.
The Journal of Organic Chemistry, 43(5), 960-962 (1978)
Tissue residues of arprinocid in chickens. 1. Depletion of residues in tissues of chickens fed carbon-14-labeled arprinocid.
T A Jacob et al.
Journal of agricultural and food chemistry, 30(2), 248-253 (1982-03-01)

Questions

Reviews

No rating value

Active Filters

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