Search Thermo Fisher Scientific
- Contact Us
- Quick Order
-
Don't have an account ? Create Account
Element Search
Structure SearchThermo Scientific Chemicals
Thiazole-2-carboxaldehyde, 95%, Thermo Scientific Chemicals
Catalog number: H63329.06
5 g, Each
Thermo Scientific Chemicals
Thiazole-2-carboxaldehyde, 95%, Thermo Scientific Chemicals
Catalog number: H63329.06
5 g, Each
Quantity
Catalog number: H63329.06
also known as H63329-06
Price (JPY)
Chemical Identifiers
CAS
10200-59-6
IUPAC Name
1,3-thiazole-2-carbaldehyde
Molecular Formula
C4H3NOS
InChI Key
ZGTFNNUASMWGTM-UHFFFAOYSA-N
SMILES
O=CC1=NC=CS1
Specifications
Specification SheetAssay (GC)
>94.0%
Description
Thiazole-2-carboxaldehyde may be used as a reactant in the following syntheses Benzothiazine N-acylhydrazones, having potential antinociceptive and anti-inflammatory activity, Thiazole-2-yl-(amino)methylphosphonate diethyl esters, Imino ester by reacting with L-leucine t-butyl ester hydrochloride. Also used in building block for taxane analogs.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Thiazole-2-carboxaldehyde may be used as a reactant in the following syntheses Benzothiazine N-acylhydrazones, having potential antinociceptive and anti-inflammatory activity, Thiazole-2-yl-(amino)methylphosphonate diethyl esters, Imino ester by reacting with L-leucine t-butyl ester hydrochloride. Also used in building block for taxane analogs.
Solubility
Fully miscible with water.
Notes
Refrigerate. Keep container tightly closed. Store away from oxidizing agent.
Thiazole-2-carboxaldehyde may be used as a reactant in the following syntheses Benzothiazine N-acylhydrazones, having potential antinociceptive and anti-inflammatory activity, Thiazole-2-yl-(amino)methylphosphonate diethyl esters, Imino ester by reacting with L-leucine t-butyl ester hydrochloride. Also used in building block for taxane analogs.
Solubility
Fully miscible with water.
Notes
Refrigerate. Keep container tightly closed. Store away from oxidizing agent.
RUO – Research Use Only
Figures
Documents & Downloads
Certificates
Search by lot number or partial lot number
Frequently asked questions (FAQs)
Citations & References
Search citations by name, author, journal title or abstract text