Skip to Content
Merck
All Photos(1)

Key Documents

235237

Sigma-Aldrich

2-Chlorophenyl phosphorodichloridate

99%

Synonym(s):

2-Chlorophenyl dichlorophosphate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
Cl2P(O)OC6H4Cl
CAS Number:
Molecular Weight:
245.43
Beilstein:
911009
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.538 (lit.)

bp

135-137 °C/12 mmHg (lit.)

density

1.491 g/mL at 25 °C (lit.)

SMILES string

Clc1ccccc1OP(Cl)(Cl)=O

InChI

1S/C6H4Cl3O2P/c7-5-3-1-2-4-6(5)11-12(8,9)10/h1-4H

InChI key

VLDPXPPHXDGHEW-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

2-Chlorophenyl phosphorodichloridate has been used in the preparation of:
  • mononucleotide building blocks
  • oligonucleotides and oligonucleotide phosphorothioates in solution

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

221.0 °F - closed cup

Flash Point(C)

105 °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

Dealkylation of nucleoside arylmethyl 2-chlorophenyl phosphates: the 2, 4-dinitrobenzyl protecting group.
Christadoulou C and Reese CB.
Tetrahedron Letters, 24(9), 951-954 (1983)
A new approach to the synthesis of oligonucleotides and their phosphorothioate analogues in solution.
Reese CB and Song Q.
Bioorganic & Medicinal Chemistry Letters, 7(21), 2787-2792 (1997)
Stereoselective chain elongation at C-3 of cysteine through 2,3-dihydrothiazoles, without racemization. Preparation of 2-amino-5-hydroxy-3-mercaptoalkanoic acid derivatives
Andre Jeanguenat and Dieter Seebach
Journal of the Chemical Society. Perkin Transactions 1, 2291-2298 (1991)

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