Skip to Content
MilliporeSigma
All Photos(1)

Documents

140333

Sigma-Aldrich

Benzyl 2,2,2-trichloroacetimidate

≥96%

Synonym(s):

2,2,2-Trichloroacetimidic acid benzyl ester

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CCl3C(=NH)OCH2C6H5
CAS Number:
Molecular Weight:
252.52
Beilstein/REAXYS Number:
2525375
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

≥96%

form

liquid

impurities

<1% benzyl alcohol

refractive index

n20/D 1.545 (lit.)

bp

106-114 °C/0.5 mmHg (lit.)

transition temp

solidification point 3-4 °C

density

1.359 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

ClC(Cl)(Cl)C(=N)OCc1ccccc1

InChI

1S/C9H8Cl3NO/c10-9(11,12)8(13)14-6-7-4-2-1-3-5-7/h1-5,13H,6H2

InChI key

HUZCTWYDQIQZPM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Benzyl 2,2,2-trichloroacetimidate was used as reagent during the synthesis of funiculosin dimethyl ether and (S)-3-(benzyloxy)-2-methylpropanal. It was used in the acid-catalyzed benzylation of hydroxy groups.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, 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

The total synthesis of scytophycin C. Part 1: stereocontrolled synthesis of the C1? C32 protected seco acid.
Paterson I, et al.
Tetrahedron, 54(39), 11935-11954 (1998)
Tetrahedron Asymmetry, 3, 1547-1547 (1992)
Studies of novel cyclitols. A synthesis of 3'O, 4'O -dimethylfuniculosin.
Williams DR, et al.
Tetrahedron Letters, 41(49), 9397-9401 (2000)

Articles

Trichloroacetimidates are also commonly employed as alcohol alkylation reagents, particularly when existing functionality is not acid sensitive.

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