ALD00352

Boc-2-methoxy-L-phenylalanine

97%

Manufacturer: Sigma Aldrich

CAS Number: 143415-63-8

Synonym(S): (S)-2-(tert-butoxycarbonylamino)-3-(2-methoxyphenyl)propanoic acid

Select a Size

Pack Size SKU Availability Price
1 G ALD00352-1-G In Stock ₹ 18,629.83

ALD00352 - 1 G

₹ 18,629.83

In Stock

Quantity

1

Base Price: ₹ 18,629.83

GST (18%): ₹ 3,353.369

Total Price: ₹ 21,983.199

Quality Level

100

Assay

97%

form

powder

reaction suitability

reaction type: Boc solid-phase peptide synthesisreagent type: ligandreaction type: C-H Activation

mp

157 °C

application(s)

peptide synthesis

storage temp.

2-8°C

SMILES string

OC([C@@H](NC(OC(C)(C)C)=O)CC1=CC=CC=C1OC)=O

InChI

1S/C15H21NO5/c1-15(2,3)21-14(19)16-11(13(17)18)9-10-7-5-6-8-12(10)20-4/h5-8,11H,9H2,1-4H3,(H,16,19)(H,17,18)/t11-/m0/s1

InChI key

QMHKMTAKTUUKEK-NSHDSACASA-N

Other Options

Image Product Name Manufacturer Price Range
50-218-1901
eMolecules​ BOC-2-METHOXY-L-PHENYLALANINE | 143415-63-8 | MFCD01860640 | 1g
eMolecules​ ₹ 52,100.05
50-175-4632
Sigma Aldrich Fine Chemicals Biosciences Boc-2-methoxy-L-phenylalanine 97% | 143415-63-8 | MFCD01860640 | 1G
Sigma Aldrich Fine Chemicals Biosciences ₹ 29,347.08
CS-0201609
Boc-2-methoxy-L-phenylalanine
ChemScene ₹ 8,641.56 - ₹ 38,929.80
AE37405
143415-63-8 | (S)-2-((tert-Butoxycarbonyl)amino)-3-(2-methoxyphenyl)propanoic acid
A2B Chem ₹ 3,422.40 - ₹ 70,501.44

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Description

  • Application: Unnatural amino acid was derived from a C-H Activation methodology developed by Jin-Quan Yu and coworkers. The Pd-mediated C-C bond formation can be made in tandem with 2-Methylpyridine (Aldrich 109835).
  • Other Notes: Ligand-Controlled C(sp3)–H Arylation and Olefination in Synthesis of Unnatural Chiral α–Amino Acids

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Compare Similar Items

Show Difference

Img

Sigma Aldrich

ALD00352

97%...


Quality Level:
100

Assay:
97%

form:
powder

reaction suitability:
reaction type: Boc solid-phase peptide synthesisreagent type: ligandreaction type: C-H Activation

mp:
157 °C

application(s):
peptide synthesis

storage temp.:
2-8°C

SMILES string:
OC([C@@H](NC(OC(C)(C)C)=O)CC1=CC=CC=C1OC)=O

InChI:
1S/C15H21NO5/c1-15(2,3)21-14(19)16-11(13(17)18)9-10-7-5-6-8-12(10)20-4/h5-8,11H,9H2,1-4H3,(H,16,19)(H,17,18)/t11-/m0/s1

InChI key:
QMHKMTAKTUUKEK-NSHDSACASA-N

Img

Sigma Aldrich

ALD00364

95% (GC)...


Quality Level:
100

Assay:
95% (GC)

form:
crystals

reaction suitability:
reaction type: click chemistry

mp:
104-110 °C

application(s):
__

storage temp.:
__

SMILES string:
FS(C1=CC=C(C(CBr)=O)C=C1)(=O)=O

InChI:
1S/C8H6BrFO3S/c9-5-8(11)6-1-3-7(4-2-6)14(10,12)13/h1-4H,5H2

InChI key:
RWHNIEOAPNZZGI-UHFFFAOYSA-N

Img

Sigma Aldrich

ALD00374

--


Quality Level:
100

Assay:
__

form:
solid

reaction suitability:
reaction type: Fmoc solid-phase peptide synthesis

mp:
__

application(s):
peptide synthesis

storage temp.:
2-8°C

SMILES string:
FC1=CC=CC(C[C@H](NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O)C(O)=O)=C1

InChI:
1S/C24H20FNO4/c25-16-7-5-6-15(12-16)13-22(23(27)28)26-24(29)30-14-21-19-10-3-1-8-17(19)18-9-2-4-11-20(18)21/h1-12,21-22H,13-14H2,(H,26,29)(H,27,28)/t22-/m0/s1

InChI key:
DWSDVARCJDOADL-QFIPXVFZSA-N

Img

Sigma Aldrich

ALD00374

--


Quality Level:
100

Assay:
__

form:
solid

reaction suitability:
reaction type: Fmoc solid-phase peptide synthesis

mp:
__

application(s):
peptide synthesis

storage temp.:
2-8°C

SMILES string:
FC1=CC=CC(C[C@H](NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O)C(O)=O)=C1

InChI:
1S/C24H20FNO4/c25-16-7-5-6-15(12-16)13-22(23(27)28)26-24(29)30-14-21-19-10-3-1-8-17(19)18-9-2-4-11-20(18)21/h1-12,21-22H,13-14H2,(H,26,29)(H,27,28)/t22-/m0/s1

InChI key:
DWSDVARCJDOADL-QFIPXVFZSA-N