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Merck
CN

287288

3-(2-Thienyl)-DL-alanine

≥98%

Synonym(s):

2-Amino-3-(2-thienyl)propionic acid

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About This Item

Empirical Formula (Hill Notation):
C7H9NO2S
CAS Number:
2021-58-1
Molecular Weight:
171.22
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
24857270
EC Number:
217-967-1
Beilstein/REAXYS Number:
82874
MDL number:
MFCD00005459

Key Documents

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Product Name

3-(2-Thienyl)-DL-alanine, ≥98%

InChI key

WTOFYLAWDLQMBZ-UHFFFAOYSA-N

InChI

1S/C7H9NO2S/c8-6(7(9)10)4-5-2-1-3-11-5/h1-3,6H,4,8H2,(H,9,10)

SMILES string

NC(Cc1cccs1)C(O)=O

assay

≥98%

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

mp

275-277 °C (dec.) (lit.)

application(s)

peptide synthesis

Quality Level

200

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Related Categories

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
0000151719
0000151719
0000087474
0000087490
0000083465

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K J Brown et al.
Antonie van Leeuwenhoek, 45(4), 531-546 (1979-01-01)
Mice fed beta-2-thienylalanine (beta-2-T) by oesophageal tube were no more susceptible to gastrointestinal tract colonization by Salmonella typhimurium or Shigella flexneri III than control mice fed water. In both beta-2-T-fed and water-fed groups, the increasing dosage of S. typhimurium, in
K J Brown et al.
Microbiology and immunology, 24(7), 603-615 (1980-01-01)
Growth comparisons were made, using Shigella, Escherichia, and Salmonella cultures, in liquid and agar-solidified defined media containing beta-2-thienylalanine (beta-2-t). The comparisons were performed to determine the nature of growth inhibition by beta-2-t under different physical growth conditions. In a plate
S Stoev et al.
Journal of peptide science : an official publication of the European Peptide Society, 5(3), 141-153 (1999-05-14)
We report the solid-phase synthesis and some pharmacological properties of 23 new analogs of arginine vasopressin (AVP) which have the Phe3 residue replaced by a broad variety of amino acids. Peptides 1-9 have at position 3: (1) the mixed aromatic/aliphatic
Uptake and incorporation of amino acids by suspension cultured mammalian cells: a comparative study involving eleven naturally-occurring and four analogue amino acids.
D N Wheatley et al.
Cytobios, 30(118), 101-126 (1981-01-01)
"Physiological phenylketonuria": a biochemical defect caused by delayed maturation of the phenylalanine hydroxylation pathway and by competition with the phenylalanine biosynthetic pathway.
K J Brown
Medical hypotheses, 6(2), 215-224 (1980-02-01)
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