15402

Boc-Dap-OH

≥98.0% (TLC)

Manufacturer: Sigma Aldrich

CAS Number: 73259-81-1

Synonym(S): (S)-2-[(tert-Butoxycarbonyl)amino]-3-aminopropionic acid, (S)-3-Amino-2-(tert-butoxycarbonyl)aminopropionic acid, (S)-3-Amino-2-(tert-butoxycarbonylamino)propanoic acid, 3-Amino-(tert-butoxycarbonyl)-L-alanine, Nα-BOC-(S)-β-aminoalanine, Nα-Boc-L-β-aminoalanine, N2-(tert-Butoxycarbonyl)-(S)-2,3-diaminopropionic acid, N2-tert-Butoxycarbonyl-L-2,3-diaminopropionic acid, Nα-Boc-L-2,3-diaminopropionic acid, Boc-Dpr-OH

Select a Size

Pack Size SKU Availability Price
1 G 15402-1-G In Stock ₹ 5,737.25
5 G 15402-5-G In Stock ₹ 21,888.15

15402 - 1 G

₹ 5,737.25

In Stock

Quantity

1

Base Price: ₹ 5,737.25

GST (18%): ₹ 1,032.705

Total Price: ₹ 6,769.955

Quality Level

100

Assay

≥98.0% (TLC)

form

solid

optical activity

[α]20/D +5.5±1°, c = 1% in methanol: water (1:1)

reaction suitability

reaction type: Boc solid-phase peptide synthesis

impurities

~3% water

mp

210 °C (dec.)

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N[C@@H](CN)C(O)=O

InChI

1S/C8H16N2O4/c1-8(2,3)14-7(13)10-5(4-9)6(11)12/h5H,4,9H2,1-3H3,(H,10,13)(H,11,12)/t5-/m0/s1

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Description

  • Application: Reactant for:Protein assembly directed by synthetic molecular recognition motifsSolid phase synthesis of gramicidin S cyclic analogs with antibiotic and hemolytic activitiesSynthesis of HCV protease inhibitor modified analogsSolid phase synthesis of peptidic V1a receptor agonistsDirected peptide assembly at lipid-water interface
  • Other Notes: Monoprotected derivative of DAP; used e.g. in the synthesis of glucosamine synthase inhibitors,[1][2] a myosin kinase inhibitor.[3] Preparation of peptides with metal complexing groups.[4]

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Sigma Aldrich

15402

≥98.0% (TLC)...


Quality Level:
100

Assay:
≥98.0% (TLC)

form:
solid

optical activity:
[α]20/D +5.5±1°, c = 1% in methanol: water (1:1)

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

impurities:
~3% water

mp:
210 °C (dec.)

application(s):
peptide synthesis

SMILES string:
CC(C)(C)OC(=O)N[C@@H](CN)C(O)=O

InChI:
1S/C8H16N2O4/c1-8(2,3)14-7(13)10-5(4-9)6(11)12/h5H,4,9H2,1-3H3,(H,10,13)(H,11,12)/t5-/m0/s1

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200

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≥97.0% (NT)

form:
__

optical activity:
__

reaction suitability:
reagent type: cross-linking reagent

impurities:
__

mp:
__

application(s):
__

SMILES string:
NCCCCCNC(OC(C)(C)C)=O

InChI:
1S/C10H22N2O2/c1-10(2,3)14-9(13)12-8-6-4-5-7-11/h4-8,11H2,1-3H3,(H,12,13)

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form:
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optical activity:
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reagent type: cross-linking reagent

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22 °C (lit.)

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SMILES string:
NCCCNC(OC(C)(C)C)=O

InChI:
1S/C8H18N2O2/c1-8(2,3)12-7(11)10-6-4-5-9/h4-6,9H2,1-3H3,(H,10,11)

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SMILES string:
COc1ccc(cc1)C(C)O

InChI:
1S/C9H12O2/c1-7(10)8-3-5-9(11-2)6-4-8/h3-7,10H,1-2H3