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Merck
모든 사진(1)

주요 문서

364517

Sigma-Aldrich

L-Tryptophan methyl ester hydrochloride

98%, for peptide synthesis

동의어(들):

(S)-Tryptophan methyl ester hydrochloride, H-(L)-Trp-OMe hydrochloride, L-(-)-Tryptophan methyl ester hydrochloride, Tryptophan methyl ester hydrochloride

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About This Item

실험식(Hill 표기법):
C12H14N2O2 · HCl
CAS Number:
Molecular Weight:
254.71
Beilstein:
4240280
EC Number:
MDL number:
UNSPSC 코드:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22

product name

L-Tryptophan methyl ester hydrochloride, 98%

Quality Level

분석

98%

광학 활성

[α]20/D +18°, c = 5 in methanol

반응 적합성

reaction type: solution phase peptide synthesis

mp

218-220 °C (lit.)

응용 분야

peptide synthesis

SMILES string

Cl.COC(=O)[C@@H](N)Cc1c[nH]c2ccccc12

InChI

1S/C12H14N2O2.ClH/c1-16-12(15)10(13)6-8-7-14-11-5-3-2-4-9(8)11;/h2-5,7,10,14H,6,13H2,1H3;1H/t10-;/m0./s1

InChI key

XNFNGGQRDXFYMM-PPHPATTJSA-N

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애플리케이션

L-Tryptophan methyl ester hydrochloride can be used as a reactant to prepare:
  • Oxamoyl derivatives of N-(2-aminobenzoyl)-L-tryptophan (dipeptides) by acylation reaction with 3,1-benzoxazinones.
  • Tadalafil (Cialis), a type-V phosphodiesterase (PDE5) inhibitor.
  • Isoroquefortine C.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

Synthesis of tadalafil (Cialis) from L-tryptophan
Xiao Sen, et al.
Tetrahedron Asymmetry, 20(18), 2090-2096 (2009)
Bruno M Schiavi et al.
The Journal of organic chemistry, 67(3), 620-624 (2002-02-22)
A short and efficient total synthesis of isoroquefortine C, the 3,12-(Z)-isomer of roquefortine C, from L-tryptophan methyl ester hydrochloride and 4(5)-(hydroxy)methylimidazole hydrochloride is described.
Synthesis of acyl derivatives of L-tryptophan containing residues of anthranilic and oxalic acids
Shemchuk LA, et al.
Russ. J. Org. Chem., 44(5), 693-696 (2008)
Christine Böttcher et al.
Journal of experimental botany, 62(12), 4267-4280 (2011-05-06)
Nine Gretchen Hagen (GH3) genes were identified in grapevine (Vitis vinifera L.) and six of these were predicted on the basis of protein sequence similarity to act as indole-3-acetic acid (IAA)-amido synthetases. The activity of these enzymes is thought to
Michael Behen et al.
Movement disorders : official journal of the Movement Disorder Society, 22(15), 2256-2262 (2007-08-22)
Symptoms in Tourette syndrome (TS) are likely related to abnormalities involving multiple neurotransmitter systems in striatal-thalamo-cortical circuitry. Although prior studies have found abnormal levels of tryptophan, serotonin, and their metabolites in blood, cerebrospinal fluid and brain tissue of TS patients

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