Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

138096

Sigma-Aldrich

Ethyl 5-chloro-2-indolecarboxylate

97%

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

About This Item

Empirical Formula (Hill Notation):
C11H10ClNO2
CAS Number:
4792-67-0
Molecular Weight:
223.66
EC Number:
225-345-6
MDL number:
MFCD00005610
UNSPSC Code:
12352100
PubChem Substance ID:
24848232
NACRES:
NA.22

Quality Level

100

Assay

97%

mp

166-168 °C (lit.)

SMILES string

CCOC(=O)c1cc2cc(Cl)ccc2[nH]1

InChI

1S/C11H10ClNO2/c1-2-15-11(14)10-6-7-5-8(12)3-4-9(7)13-10/h3-6,13H,2H2,1H3

InChI key

LWKIFKYHCJAIAB-UHFFFAOYSA-N

Application

Ethyl 5-chloro-2-indolecarboxylate was used in the synthesis of anti-allergic agents.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBF7846V
STBF0871V
STBC8464V
STBC3974V
STBB0463V

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

Y Honma et al.
Journal of medicinal chemistry, 27(2), 125-128 (1984-02-01)
A series of N-tetrazolylpyridinecarboxamides was prepared and evaluated for antiallergic activity by the passive cutaneous anaphylaxis (PCA) assay. From the structure-activity relationships (SAR) of this class of compounds, it was revealed that the N-tetrazolylcarbamoyl group as an acidic functionality is

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