MedKoo Cat#: 596547 | Name: Thiazolylalanine
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Thiazolylalanine is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

Chemical Structure

Thiazolylalanine
Thiazolylalanine
CAS#119433-80-6

Theoretical Analysis

MedKoo Cat#: 596547

Name: Thiazolylalanine

CAS#: 119433-80-6

Chemical Formula: C6H8N2O2S

Exact Mass: 172.0306

Molecular Weight: 172.20

Elemental Analysis: C, 41.85; H, 4.68; N, 16.27; O, 18.58; S, 18.62

Price and Availability

Size Price Availability Quantity
250mg USD 280.00
1g USD 510.00
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Related CAS #
No Data
Synonym
Thiazolylalanine; l-Thiazolylalanine; Thiazolylalanine, l;
IUPAC/Chemical Name
(S)-2-amino-3-(thiazol-4-yl)propanoic acid
InChi Key
WBZIGVCQRXJYQD-YFKPBYRVSA-N
InChi Code
InChI=1S/C6H8N2O2S/c7-5(6(9)10)1-4-2-11-3-8-4/h2-3,5H,1,7H2,(H,9,10)/t5-/m0/s1
SMILES Code
O=C(O)[C@@H](N)CC1=CSC=N1
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 172.20 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Mennen SM, Blank JT, Tran-Dubé MB, Imbriglio JE, Miller SJ. A peptide-catalyzed asymmetric Stetter reaction. Chem Commun (Camb). 2005 Jan 14;(2):195-7. Epub 2004 Nov 29. PubMed PMID: 15724183. 2: Mennen SM, Gipson JD, Kim YR, Miller SJ. Thiazolylalanine-derived catalysts for enantioselective intermolecular aldehyde-imine cross-couplings. J Am Chem Soc. 2005 Feb 16;127(6):1654-5. PubMed PMID: 15700996. 3: Heyl DL, Dandabathula M, Kurtz KR, Mousigian C. Opioid receptor binding requirements for the delta-selective peptide deltorphin. I: Phe3 replacement with ring-substituted and heterocyclic amino acids. J Med Chem. 1995 Mar 31;38(7):1242-6. PubMed PMID: 7707326. 4: Hashimoto N, Fujioka T, Hayashi K, Odaguchi K, Toyoda T, Nakamura M, Hirano K. Renin inhibitor: relationship between molecular structure and oral absorption. Pharm Res. 1994 Oct;11(10):1443-7. PubMed PMID: 7855049.