Skip to Content
Merck
All Photos(2)

Documents

193496

Sigma-Aldrich

2-Iodobenzyl chloride

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
IC6H4CH2Cl
CAS Number:
Molecular Weight:
252.48
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

powder

refractive index

n20/D 1.635 (lit.)

bp

147-149 °C/32 mmHg (lit.)

mp

29-31 °C (lit.)

SMILES string

ClCc1ccccc1I

InChI

1S/C7H6ClI/c8-5-6-3-1-2-4-7(6)9/h1-4H,5H2

InChI key

FTMNWZHKQGKKAU-UHFFFAOYSA-N

Related Categories

Application

2-Iodobenzyl chloride was used in the synthesis of:
  • succinimido[3,4-b]indane
  • 1,2,3,4,5,6-hexahydro-1,5-methano-3-benzazocine-2,4-dione
  • 1-(2-iodobenzyi)-1,1-diethylamine
  • 1-(2-iodobenzyl)pyrrolidine
  • 1-(2-iodobenzyl)piperidine
  • 1-(2-iodobenzyl)hexahydroazepine
  • 4-(2-iodobenzyl)morpholine
  • 4-(2-iodobenzyl)thiomorpholine
  • 1-benzoyl-4-(2-iodobenzyl)piperazine
  • 1-(2-iodobenzyl)indole-2-carbaldehyde

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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

An Approach to α-substituted Amines.
Williams L, et al.
Tetrahedron, 50(48), 13697-13708 (1994)
Sushama A. Dandekar et al.
The Journal of organic chemistry, 64(5), 1543-1553 (2001-10-25)
The tricyclic title compounds, 4 and 5, were synthesized by initial alkylation of the lithium monoenolates of N,N,N',N'-tetramethylbutanediamide (6) and N,N,N',N'-tetramethylpentanediamide (19) with 2-iodobenzyl chloride in liquid NH(3) at -60 degrees C to afford 2-(2-iodobenzyl)-N,N,N',N'-tetramethylbutanediamide (9) and 2-(2-iodobenzyl)-N,N,N',N'-tetramethylpentanediamide (20) in
1-Azatriene cyclisation as a route to annelated pyrido [4, 3-b] indoles.
Gilchrist TL ,et al.
Tetrahedron, 53(12), 4447-4456 (1997)

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